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US20150018374A1 - Fungicidal pyrazole mixtures - Google Patents

Fungicidal pyrazole mixtures Download PDF

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Publication number
US20150018374A1
US20150018374A1 US14/374,315 US201314374315A US2015018374A1 US 20150018374 A1 US20150018374 A1 US 20150018374A1 US 201314374315 A US201314374315 A US 201314374315A US 2015018374 A1 US2015018374 A1 US 2015018374A1
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Prior art keywords
fungicides
methyl
compound
formula
compounds
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US14/374,315
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US10015966B2 (en
Inventor
Andrew Edmund Taggi
Jeffrey Keith Long
James Francis Bereznak
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FMC Corp
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EI Du Pont de Nemours and Co
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Assigned to E. I. DUPONT DE NEMOURS AND COMPANY reassignment E. I. DUPONT DE NEMOURS AND COMPANY ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: LONG, JEFFREY KEITH, TAGGI, ANDREW EDMUND, BEREZNAK, JAMES FRANCIS
Publication of US20150018374A1 publication Critical patent/US20150018374A1/en
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    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
    • A01N37/10—Aromatic or araliphatic carboxylic acids, or thio analogues thereof; Derivatives thereof
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
    • A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
    • A01N37/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
    • A01N37/36—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
    • A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
    • A01N43/06—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings
    • A01N43/10—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings with sulfur as the ring hetero atom
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
    • A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
    • A01N43/50—1,3-Diazoles; Hydrogenated 1,3-diazoles
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
    • A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
    • A01N43/60—1,4-Diazines; Hydrogenated 1,4-diazines
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/713—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with four or more nitrogen atoms as the only ring hetero atoms
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
    • A01N43/74—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
    • A01N43/76—1,3-Oxazoles; Hydrogenated 1,3-oxazoles
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
    • A01N43/74—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
    • A01N43/78—1,3-Thiazoles; Hydrogenated 1,3-thiazoles
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
    • A01N43/80—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
    • A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
    • A01N47/18—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, directly attached to a heterocyclic or cycloaliphatic ring
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C255/00—Carboxylic acid nitriles
    • C07C255/01—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms
    • C07C255/32—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms having cyano groups bound to acyclic carbon atoms of a carbon skeleton containing at least one six-membered aromatic ring
    • C07C255/40—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms having cyano groups bound to acyclic carbon atoms of a carbon skeleton containing at least one six-membered aromatic ring the carbon skeleton being further substituted by doubly-bound oxygen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
    • C07C323/23—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton
    • C07C323/24—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton
    • C07C323/29—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton containing six-membered aromatic rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C331/00—Derivatives of thiocyanic acid or of isothiocyanic acid
    • C07C331/16—Isothiocyanates
    • C07C331/28—Isothiocyanates having isothiocyanate groups bound to carbon atoms of six-membered aromatic rings
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms

Definitions

  • This invention relates to certain pyrazole derivatives, their N-oxides and salts, to process intermediates for their preparation and to mixtures and compositions comprising such pyrazole derivatives and methods for using such pyrazole derivatives and their mixtures and compositions as fungicides.
  • This invention relates to a fungicidal composition (i.e. combination, mixture) comprising
  • This invention also relates to a fungicidal composition
  • a fungicidal composition comprising: (a) at least one compound selected from the compounds of Formula 1, (b) at least one fungicidal compound selected from Formulae B1 through B13 and salts thereof described above, and further comprising (c) at least one additional compound or agent that is biologically active.
  • This invention also relates to a composition
  • a composition comprising one of the aforesaid compositions comprising components (a) and (b) and at least one additional component selected from the group consisting of surfactants, solid diluents and liquid diluents.
  • This invention also relates to a method for controlling plant diseases caused by fungal plant pathogens comprising applying to the plant or portion thereof, or to the plant seed, a fungicidally effective amount of one of the aforesaid compositions.
  • the aforedescribed method can also be described as a method for protecting a plant or plant seed from diseases caused by fungal pathogens comprising applying a fungicidally effective amount of one of the aforesaid compositions to the plant (or portion thereof) or plant seed (directly or through the environment (e.g., growing medium) of the plant or plant seed).
  • This invention also relates to a compound of Formula 1 described above, or an N-oxide or salt thereof.
  • This invention further relates to a fungicidal composition comprising a compound of Formula 1, or an N-oxide or salt thereof, and at least one additional component selected from the group consisting of surfactants, solid diluents and liquid diluents.
  • This invention also further relates to a method for protecting a plant or plant seed from diseases caused by fungal pathogens comprising a fungicidally effective amount of a compound of Formula 1, or an N-oxide or salt thereof, to the plant or plant seed.
  • This invention further relates to a compound of Formula 14,
  • R 3 is Cl or Br.
  • This invention further relates to a compound of Formula 17,
  • This invention further relates to a compound of Formula 20,
  • R 1 is F, Cl or Br
  • R 2 is H or F, particularly wherein R 1 is Br and R 2 is F.
  • This invention further relates to a compound of Formula 22,
  • R 1 is F, Cl or Br
  • R 2 is H or F
  • R 3 is Cl or Br
  • M is Na or K.
  • Compounds of Formulae 14, 17, 20 and 22 can be used as process intermediates to prepare compounds of Formula 1, which are useful as component (a) in the present compositions.
  • compositions comprising, “comprising,” “includes,” “including,” “has,” “having,” “contains”, “containing,” “characterized by” or any other variation thereof, are intended to cover a non-exclusive inclusion, subject to any limitation explicitly indicated.
  • a composition, mixture, process or method that comprises a list of elements is not necessarily limited to only those elements but may include other elements not expressly listed or inherent to such composition, mixture, process or method.
  • transitional phrase “consisting essentially of” is used to define a composition or method that includes materials, steps, features, components, or elements, in addition to those literally disclosed, provided that these additional materials, steps, features, components, or elements do not materially affect the basic and novel characteristic(s) of the claimed invention.
  • the term “consisting essentially of” occupies a middle ground between “comprising” and “consisting of”.
  • plant includes members of Kingdom Plantae, particularly seed plants (Spermatopsida), at all life stages, including young plants (e.g., germinating seeds developing into seedlings) and mature, reproductive stages (e.g., plants producing flowers and seeds).
  • Portions of plants include geotropic members typically growing beneath the surface of the growing medium (e.g., soil), such as roots, tubers, bulbs and corms, and also members growing above the growing medium, such as foliage (including stems and leaves), flowers, fruits and seeds.
  • seedling used either alone or in a combination of words means a young plant developing from the embryo of a seed.
  • Registry Number refers to Chemical Abstracts Registry Number.
  • a single bond drawn as a wavy line denote that either the E or Z isomer or a mixture of E and Z isomers may be present.
  • a dashed line perpendicularly traversing a bond denotes that the bond connects the substituent fragment to the remainder of a molecule (e.g., R b1 in Formula B2).
  • Compounds relevant to the compositions and methods of this invention can exist as one or more stereoisomers.
  • the various stereoisomers include enantiomers, diastereomers, atropisomers and geometric isomers.
  • one stereoisomer may be more active and/or may exhibit beneficial effects when enriched relative to the other stereoisomer(s) or when separated from the other stereoisomer(s). Additionally, the skilled artisan knows how to separate, enrich, and/or to selectively prepare said stereoisomers.
  • the compounds in the compositions of this invention may be present as a mixture of stereoisomers, individual stereoisomers or as an optically active form.
  • salts of chemical compounds are in equilibrium with their corresponding nonsalt forms, salts share the biological utility of the nonsalt forms.
  • the salts of the compounds of Formula 1 include acid-addition salts with inorganic or organic acids such as hydrobromic, hydrochloric, nitric, phosphoric, sulfuric, acetic, butyric, fumaric, lactic, maleic, malonic, oxalic, propionic, salicylic, tartaric, 4-toluenesulfonic or valeric acids.
  • the present invention relates to mixtures of compounds selected from Formula 1, N-oxides and agriculturally suitable salts thereof.
  • biologically similar salt forms can exist for many of the compounds of Formulae B1 through B13.
  • Non-crystalline forms include embodiments which are solids such as waxes and gums as well as embodiments which are liquids such as solutions and melts.
  • Crystalline forms include embodiments which represent essentially a single crystal type and embodiments which represent a mixture of polymorphs (i.e. different crystalline types).
  • polymorph refers to a particular crystalline form of a chemical compound that can crystallize in different crystalline forms, these forms having different arrangements and/or conformations of the molecules in the crystal lattice.
  • polymorphs can have the same chemical composition, they can also differ in composition due the presence or absence of co-crystallized water or other molecules, which can be weakly or strongly bound in the lattice. Polymorphs can differ in such chemical, physical and biological properties as crystal shape, density, hardness, color, chemical stability, melting point, hygroscopicity, suspensibility, dissolution rate and biological availability.
  • beneficial effects e.g., suitability for preparation of useful formulations, improved biological performance
  • Preparation and isolation of a particular polymorph of a compound represented by Formula 1 can be achieved by methods known to those skilled in the art including, for example, crystallization using selected solvents and temperatures.
  • Compounds of Formulae B1 through B13, including salts thereof, can also typically exist in more than one form.
  • reference to Formula 1 includes N-oxides and salts thereof unless otherwise indicated, and reference to “a compound of Formula 1” includes the definitions of substituents specified in the Summary of the Invention unless further defined in the Embodiments. Furthermore, reference to Formulae B1 through B13 includes salts thereof unless otherwise indicated.
  • composition comprising components (a) and (b) described in the Summary of the Invention wherein in Formula 1, R 2 is F.
  • composition comprising components (a) and (b) described in the Summary of the Invention wherein in Formula 1, R 2 is H.
  • composition comprising components (a) and (b) described in the Summary of the Invention or Embodiment 1 or 2 wherein component (a) does not comprise an N-oxide of a compound of Formula 1.
  • composition comprising components (a) and (b) described in the Summary of the Invention or Embodiment 3 wherein component (a) comprises a compound selected from the group consisting of
  • composition of Embodiment 4 wherein component (a) comprises Compound 1.
  • composition of Embodiment 4 wherein component (a) comprises Compound 2.
  • composition of Embodiment 4 wherein component (a) comprises Compound 3.
  • composition of Embodiment 4 wherein component (a) comprises Compound 4.
  • composition of Embodiment 4 wherein component (a) comprises Compound 5.
  • composition of Embodiment 4 wherein component (a) comprises Compound 6.
  • composition of Embodiment 4 wherein component (a) comprises Compound 7.
  • composition of Embodiment 4 wherein component (a) comprises Compound 8.
  • composition of Embodiment 4 wherein component (a) comprises Compound 9.
  • composition of Embodiment 4 wherein component (a) comprises Compound 10.
  • composition of Embodiment 4 wherein component (a) comprises Compound 11.
  • composition of Embodiment 4 wherein component (a) comprises Compound 12.
  • composition comprising components (a) and (b) described in the Summary of the Invention or any one of Embodiments 1 through 16 wherein component (b) comprises at least one fungicidal compound selected from (b1).
  • composition comprising components (a) and (b) described in the Summary of the Invention or any one of Embodiments 1 through 17 wherein component (b) comprises at least one fungicidal compound selected from (b1a).
  • composition comprising components (a) and (b) described in the Summary of the Invention or any one of Embodiments 1 through 17a wherein component (b) comprises at least one fungicidal compound selected from (b1b).
  • composition comprising components (a) and (b) described in the Summary of the Invention or any one of Embodiments 1 through 17b wherein component (b) comprises at least one fungicidal compound selected from (b2).
  • composition comprising components (a) and (b) described in the Summary of the Invention or any one of Embodiments 1 through 18 wherein component (b) comprises at least one fungicidal compound selected from (b3).
  • composition comprising components (a) and (b) described in the Summary of the Invention or any one of Embodiments 1 through 19 wherein component (b) comprises at least one fungicidal compound selected from (b4).
  • composition comprising components (a) and (b) described in the Summary of the Invention or any one of Embodiments 1 through 20 wherein component (b) comprises at least one fungicidal compound selected from (b5).
  • composition comprising components (a) and (b) described in the Summary of the Invention or any one of Embodiments 1 through 21 wherein component (b) comprises at least one fungicidal compound selected from (b6).
  • composition comprising components (a) and (b) described in the Summary of the Invention or any one of Embodiments 1 through 22 wherein component (b) comprises at least one fungicidal compound selected from (b7).
  • composition comprising components (a) and (b) described in the Summary of the Invention or any one of Embodiments 1 through 23 wherein component (b) comprises at least one fungicidal compound selected from (b8).
  • composition comprising components (a) and (b) described in the Summary of the Invention or any one of Embodiments 1 through 24 wherein component (b) comprises at least one fungicidal compound selected from (b9).
  • composition comprising components (a) and (b) described in the Summary of the Invention or any one of Embodiments 1 through 25 wherein component (b) comprises at least one fungicidal compound selected from (b10).
  • composition comprising components (a) and (b) described in the Summary of the Invention or any one of Embodiments 1 through 26 wherein component (b) comprises at least one fungicidal compound selected from (b10a).
  • composition comprising components (a) and (b) described in the Summary of the Invention or any one of Embodiments 1 through 26a wherein component (b) comprises at least one fungicidal compound selected from (b10b).
  • composition comprising components (a) and (b) described in the Summary of the Invention or any one of Embodiments 1 through 26b wherein component (b) comprises at least one fungicidal compound selected from (b11).
  • composition comprising components (a) and (b) described in the Summary of the Invention or any one of Embodiments 1 through 27 wherein component (b) comprises at least one fungicidal compound selected from (b12).
  • composition comprising components (a) and (b) described in the Summary of the Invention or any one of Embodiments 1 through 28 wherein component (b) comprises at least one fungicidal compound selected from (b13).
  • composition comprising components (a) and (b) described in the Summary of the Invention or any one of Embodiments 1 through 28a further comprising (c) least one additional compound or agent that is biologically active.
  • component (c) comprises at least one fungicidal compound selected from the group consisting of:
  • component (c) includes at least one compound selected from acibenzolar-S-methyl, aldimorph, ametoctradin, amisulbrom, anilazine, azaconazole, azoxystrobin, benalaxyl, benalaxyl-M, benodanil, benomyl, benthiavalicarb, benthiavalicarb-isopropyl, bethoxazin, binapacryl, biphenyl, bitertanol, bixafen, blasticidin-S, boscalid, bromuconazole, bupirimate, buthiobate, carboxin, carpropamid, captafol, captan, carbendazim, chloroneb, chlorothalonil, chlozolinate, clotrimazole, copper salts (such as Bordeaux mixture (tribasic copper sulfate), copper hydroxide and
  • component (c) includes at least one compound selected from azoxystrobin, bixafen, boscalid (nicobifen), bromuconazole, carbendazim, chlorothalonil, cyflufenamid, cyproconazole, difenoconazole, dimoxystrobin, epoxiconazole, etaconazole, famoxadone, fenbuconazole, fenpropidin, fenpropimorph, fluopyram, flusilazole, fluxapyroxad, hexaconazole, ipconazole, isopyrazam, kresoxim-methyl, metaconazole, metominostrobin/fenominostrobin, metrafenone, myclobutanil, penconazole, penthiopyrad, picoxystrobin, prochloraz, propiconazole, proquinazi
  • component (c) includes at least one compound selected from azoxystrobin, bixafen, boscalid, cyflufenamid, cyproconazole, difenconazole, epoxiconazole, fluopyram, isopyrazam, kresoxim-methyl, metaconazole, metrafenone, myclobutanil, penthiopyrad, picoxystrobin, pyraclostrobin, pyrametrostrobin, pyraoxystrobin, pyriofenone, proquinazid, prothioconazole, quinoxyfen, sedaxane, tebuconazole and trifloxystrobin.
  • composition comprising components (a) and (b) described in the Summary of the Invention or any one of Embodiments 1 through 33 wherein the composition further comprises in component (c) at least one invertebrate pest control compound or agent.
  • composition comprising components (a) and (b) described in the Summary of the Invention or any one of Embodiments 1 through 34 wherein component (b1) is (b1a) (i.e. Formula B1a)
  • Embodiments of this invention can be combined in any manner.
  • embodiments of this invention including Embodiments 1-34 above as well as any other embodiments described herein, and any combination thereof, pertain to the methods of the present invention.
  • embodiments of the invention described herein and their combinations pertain to compounds of Formula 1 and intermediates for their preparation, such as compounds of Formulae 14, 17, 20 and 22.
  • component (a) comprises a compound of Formula 1 or a salt thereof.
  • compositions of the present invention comprising a composition (e.g., in a fungicidally effective amount) of any one of Embodiments 1 through 34, and at least one additional component selected from the group consisting of surfactants, solid diluents and liquid diluents.
  • Embodiments of the invention further include methods for controlling plant diseases caused by fungal plant pathogens comprising applying to the plant or portion thereof, or to the plant seed or seedling, a fungicidally effective amount of a composition any one of Embodiments 1 through 34, (e.g., as a composition including formulation ingredients as described herein).
  • Embodiments of the invention also include methods for protecting a plant or plant seed from diseases caused by fungal pathogens comprising applying a fungicidally effective amount of a composition of any one of Embodiments 1 through 34 to the plant or plant seed.
  • Some embodiments of the invention involve control of a plant disease or protection from a plant disease that primarily afflicts plant foliage and/or applying the composition of the invention to plant foliage (i.e. plants instead of seeds).
  • the preferred methods of use include those involving the above preferred compositions; and the diseases controlled with particular effectiveness include plant diseases caused by fungal plant pathogens.
  • Combinations of fungicides used in accordance with this invention can facilitate disease control and retard resistance development.
  • an aspect of the present invention is directed at a composition
  • a composition comprising as component (a) at least one compound selected from Formula 1, N-oxides, and salts thereof.
  • component (a) at least one compound selected from Formula 1, N-oxides, and salts thereof.
  • One or more of the following methods and variations as described in Schemes 1-16 can be used to prepare the compounds of Formula 1.
  • the definitions of R 1 , R 2 , R 3 , R 32 and M in the compounds of Formulae 1-23 below are as defined above in the Summary of the Invention unless otherwise noted.
  • Formulae 6a and 6b are various subsets of Formula 6;
  • Formula 10a is a subset of Formula 10;
  • Formula 17a is a tautomeric subset of Formula 17.
  • Substituents for each subset formula are as defined for its parent formula unless otherwise noted.
  • compounds of Formula 1 can be prepared by the reaction of 1H-pyrazole compounds of Formula 2 with various methylating agents (e.g., Formula 3), such as iodomethane, methyl sulfonates (e.g., methyl mesylate (OMs) or tosylate (OTs)) or trimethyl phosphate, preferably in the presence of an organic or inorganic base such as 1,8-diazabicyclo[5.4.0]undec-7-ene, potassium carbonate or potassium hydroxide, and in a solvent such as N,N-dimethylformamide (DMF), tetrahydrofuran (THF), toluene or water.
  • methylating agents e.g., Formula 3
  • iodomethane e.g., methyl mesylate (OMs) or tosylate (OTs)
  • OMs methyl mesylate
  • OTs tosylate
  • trimethyl phosphate preferably in the presence of an
  • compounds of Formula 1 can be prepared by the reaction of compounds of Formula 4 with aromatic compounds of Formula 5 containing a leaving group G (e.g., halogen or (halo)alkylsulfonate), optionally in the presence of a metal catalyst, and generally in the presence of a base and a polar aprotic solvent such as N,N-dimethylformamide or dimethyl sulfoxide.
  • a leaving group G e.g., halogen or (halo)alkylsulfonate
  • a metal catalyst e.g., halogen or (halo)alkylsulfonate
  • a metal catalyst e.g., metal or metal salt
  • G is Br or I or a sulfonate such as OS(O) 2 CF 3 or OS(O) 2 (CF 2 ) 3 CF 3 .
  • copper salt complexes e.g., CuI with N,N-dimethylethylenediamine, proline or bipyridyl
  • palladium complexes e.g., tris-(dibenzylideneacetone)dipalladium(0)
  • palladium salts e.g., palladium acetate
  • ligands such as 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (i.e. “Xantphos”), 2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl (i.e.
  • Xphos 2,2′-bis(diphenylphosphino)-1, F-binaphthalene
  • BINAP 2,2′-bis(diphenylphosphino)-1, F-binaphthalene
  • a base such as potassium carbonate, cesium carbonate, sodium phenoxide or sodium tert-butoxide
  • solvent such as N,N-dimethylformamide, 1,2-dimethoxyethane, dimethyl sulfoxide, 1,4-dioxane or toluene, optionally mixed with alcohols such as ethanol
  • compounds of Formula 1 can be prepared by reaction of compounds of Formula 6 (i.e.
  • compounds of Formula 6 wherein G is Br or I can be prepared by reaction of 5-aminopyrazoles of Formula 4 under diazotization conditions either in the presence of, or followed by combination with, copper salts containing bromide or iodide.
  • addition of tert-butyl nitrite to a solution of a 5-aminopyrazole of Formula 4 in the presence of CuBr 2 in a solvent such as acetonitrile provides the corresponding 5-bromopyrazole of Formula 6.
  • a 5-aminopyrazole of Formula 4 can be converted to a diazonium salt and then to a corresponding 5-halopyrazole of Formula 6 by treatment with sodium nitrite in solvents such as water, acetic acid or trifluoroacetic acid, in the presence of a mineral acid typically containing the same halide atom (such as aqueous HI solution for G being I), followed by treatment with the corresponding copper(I) or copper(II) salt according to general procedures well known to those skilled in the art.
  • solvents such as water, acetic acid or trifluoroacetic acid
  • 5-bromopyrazoles of Formula 6a i.e. Formula 6 wherein G is Br
  • 5-bromopyrazoles of Formula 8 can be prepared by reacting 5-hydroxypyrazoles of Formula 8 with phosphorus tribromide as described in Tetrahedron Lett. 2000, 41(24), 4713.
  • 5-hydroxypyrazoles of Formula 8 can also be used to prepare 5-fluoroalkylsulfonyl (e.g., 5-trifluoromethanesulfonyl, 5-nonafluorobutylsulfonyl) pyrazoles of Formula 6b (i.e. Formula 6 wherein G is fluoroalkylsulfonyloxy) as described in Synlett 2004, 5, 795.
  • 5-fluoroalkylsulfonyl e.g., 5-trifluoromethanesulfonyl, 5-nonafluorobutylsulfonyl
  • Formula 6b i.e. Formula 6 wherein G is fluoroalkylsulfonyloxy
  • compounds of Formula 1 can be prepared by reaction of 4-bromo or iodo pyrazoles of Formula 9 with organometallic compounds of Formula 10 under transition-metal-catalyzed cross-coupling reaction conditions.
  • a palladium or nickel catalyst having appropriate ligands (e.g., triphenylphosphine (PPh 3 ), dibenz
  • a substituted aryl boronic acid or derivative e.g., Formula 10 wherein M is B(OH) 2 , B(OC(CH 3 ) 2 C(CH 3 ) 2 O)) or B(O-i-Pr) 3 ⁇ Li ⁇ reacts with a 4-bromo- or 4-iodopyrazole of Formula 9 in the presence of dichlorobis(triphenylphosphine) palladium(II) and aqueous base such as sodium carbonate or potassium hydroxide, in solvents such as 1,4-dioxane, 1,2-dimethoxyethane, toluene or ethyl alcohol, or under anhydrous conditions with a ligand such as phosphine oxide or phosphite ligand (e.g., diphenylphosphine oxide) and potassium fluoride in a solvent such as 1,4-dioxane (see Angewandte Chemie, International Edition 2008,
  • compounds of Formula 4 can be prepared by reacting compounds of Formula 11 with compounds of Formula 10a (e.g., compounds of Formula 10 wherein M is B(OH) 2 ) using transition-metal-catalyzed cross-coupling reaction conditions as described for the method of Scheme 7.
  • compounds of Formula 10a e.g., compounds of Formula 10 wherein M is B(OH) 2
  • transition-metal-catalyzed cross-coupling reaction conditions as described for the method of Scheme 7.
  • pyrazoles of Formula 9 wherein G is Br or I are readily prepared by the reaction of pyrazoles unsubstituted at the 4-position (Formula 12) with halogenating reagents such as bromine, sodium bromite, N-bromosuccinimide (NBS) or N-iodosuccinimide (NIS), in solvents such as acetic acid, acetonitrile, N,N-dimethylformamide, N,N-dimethylacetamide or 1,4-dioxane, or a mixture of water with the aforementioned solvents, at temperatures ranging from ambient to the boiling point of the solvent.
  • halogenating reagents such as bromine, sodium bromite, N-bromosuccinimide (NBS) or N-iodosuccinimide (NIS)
  • solvents such as acetic acid, acetonitrile, N,N-dimethylformamide, N,N-dimethylacetamide or 1,4-
  • the pyrazole of Formula 13 can be converted into intermediates of Formula 11 which are useful for preparing compounds of Formula 4 as depicted in Scheme 8.
  • the compound of Formula 13 not only can be prepared by methods known in the art, but is also commercially available.
  • compounds of Formula 12 can be prepared from corresponding compounds of Formula 13 by procedures analogous to those used for the method of Scheme 2.
  • Compounds of Formula 13 are commercially available or can be prepared by methods known in the art.
  • compounds of Formula 1 can be prepared by condensing compounds of Formula 17 with methylhydrazine (Formula 15) in a solvent such as ethanol or methanol and optionally in the presence of an acid or base catalyst such as acetic acid, piperidine or sodium methoxide, according to general procedures known in the art.
  • a solvent such as ethanol or methanol
  • an acid or base catalyst such as acetic acid, piperidine or sodium methoxide
  • compounds of Formula 17 (wherein, R 32 is H or lower alkyl such as CH 3 , CH 2 CH 3 or (CH 2 ) 2 CH 3 ) can be prepared by reaction of corresponding ketene dithioacetal compounds of Formula 18 with compounds of Formula 19 optionally in the presence of a base, such as sodium hydride or ethylmagnesium chloride, in solvents such as toluene, tetrahydrofuran or dimethoxymethane, at temperatures ranging from ⁇ 10° C. to the boiling point of the solvent. See, for example, J. Heterocycl. Chem. 1975, 12(1), 139. Methods useful for preparing compounds of Formula 18 are known in the art.
  • compounds of Formula 17 wherein R 32 is lower alkyl (e.g., methyl, ethyl, n-propyl) and Formula 17a i.e. tautomer of Formula 17 wherein R 32 is H
  • R 32 is lower alkyl
  • Formula 17a i.e. tautomer of Formula 17 wherein R 32 is H
  • the intermediate compounds of Formula 22 can either be used in situ as is illustrated by Step C of Synthesis Example 1 or isolated before further conversion as is illustrated by Steps A and B of Synthesis Example 2.
  • Bases useful for preparing compounds of Formula 22 include hydrides, alkoxides, hydroxides or carbonates of sodium or potassium, such as sodium hydride, potassium tert-butoxide, sodium ethoxide, potassium hydroxide, sodium hydroxide or potassium carbonate.
  • Amine bases e.g., triethylamine or N,N-diisopropylethylamine
  • solvents are useful, such as tetrahydrofuran, ether, toluene, N,N-dimethylformamide, alcohols (e.g., ethanol), esters (e.g., ethyl acetate or isopropyl acetate), or mixtures thereof.
  • Solvents are chosen for compatibility with the base selected, as is well-known in the art. Reaction temperatures can range from ⁇ 78° C. to the boiling point of the solvent.
  • One useful mixture of base and solvent is potassium tert-butoxide in tetrahydrofuran, to which at ⁇ 70 to 0° C.
  • the salt compound of Formula 22 can be acidified to form the ketothioamide compound of Formula 17a or alkylated with R 32 X 1 (Formula 23) wherein R 32 is lower alkyl (e.g., methyl, ethyl, n-propyl) and X 1 is a nucleofuge (i.e. a nucleophilic reaction leaving group such as Br, I, OS(O) 2 CH 3 ) to form the corresponding compound of Formula 17.
  • R 32 is lower alkyl (e.g., methyl, ethyl, n-propyl)
  • X 1 is a nucleofuge (i.e. a nucleophilic reaction leaving group such as Br, I, OS(O) 2 CH 3 ) to form the corresponding compound of Formula 17.
  • Ketothioamides of Formula 17a can also be prepared by allowing the corresponding ketoamides to react with sulfurizing agents such as Lawesson's reagent or P 2 S 5 ; see, for example, Helv. Chim. Act. 1998, 81(7), 1207.
  • sulfurizing agents such as Lawesson's reagent or P 2 S 5 ; see, for example, Helv. Chim. Act. 1998, 81(7), 1207.
  • the aqueous phase was acidified and extracted with ethyl acetate.
  • the ethyl acetate phase was dried and concentrated under reduced pressure to provide the intermediate compound ⁇ -acetyl-2-bromo-4-fluorobenzeneacetonitrile as a crude oil.
  • Step C Preparation of 4-(2-Bromo-4-fluorophenyl)-N-(2-chloro-6-fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine
  • Step B) the product of Step B) (0.57 g, 3.0 mmol) in THF (10 mL) was added over 6 minutes, and stirring was continued for 15 minutes to provide a reaction mixture containing the intermediate compound 3-(2-bromo-4-fluorophenyl)-4-[(2-chloro-6-fluorophenyl)amino]-4-mercapto-3-buten-2-one potassium salt (1:1), which is the potassium salt of ⁇ -acetyl-2-bromo-N-(2-chloro-6-fluorophenyl)-4-fluorobenzeneethanethioamide.
  • Step A Preparation of 3-(2-Bromo-4-fluorophenyl)-4-[(2,6-difluorophenyl)amino]-4-mercapto-3-buten-2-one potassium salt (1:1)
  • the reaction mixture was a light yellow solution at 12° C.
  • the reaction mixture was stirred for 30 min at 12-16° C.
  • the reaction mixture was then cooled to 3° C., and a solution of 1,3-difluoro-2-isothiocyanatobenzene (17.4 g, 102 mmol) in methyl tert-butyl ether (50 mL) was added over 20 min while maintaining the temperature of the reaction mixture between 3 and 5° C.
  • the resulting yellow slurry was then slowly warmed to 12° C. over 90 min.
  • the mixture was diluted with hexanes (100 mL) and cooled to 8° C., and then the solid product was isolated by filtration.
  • the product was dried in a vacuum oven at 70° C. overnight to provide the title product as a yellow solid (32.3 g).
  • Step B Preparation of 4-(2-Bromo-4-fluorophenyl)-N-(2,6-difluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine
  • Tables 2-5 disclose specific compounds useful as process intermediates for preparing compounds of Formula 1, N-oxides, and salts thereof.
  • the “Note” column in these tables references physical property data (e.g., 1 H NMR spectra, MS parent ion(s), melting ranges) for representative compounds.
  • Mass spectra (MS) are reported as the molecular weight of the highest isotopic abundance parent ion (M+1) formed by addition of H + (molecular weight of 1) to the molecule, observed by mass spectrometry using atmospheric pressure chemical ionization (AP + ).
  • AP + atmospheric pressure chemical ionization
  • the presence of molecular ions containing one or more higher atomic weight isotopes of lower abundance e.g., 37 Cl, 81 Br
  • the M ⁇ 1 ion is also reported.
  • compounds of Formula 14 are useful process intermediates for preparing compounds of Formula 4 as intermediates to compounds of Formula 1, which are useful as component (a) in the present composition.
  • Illustrative of compounds of Formula 14 are those specifically disclosed in Table 2.
  • compounds of Formula 17 including Formula 17a are useful process intermediates for preparing compounds of Formula 1, which are useful as component (a) in the present composition.
  • Illustrative of compounds of Formulae 17 and 17a are those specifically disclosed in Table 3a and 3b.
  • R 1 R 2 R 3 Note R 32 is CH 3 .
  • F H Cl Cl H Cl Br H Cl F H Br Cl H Br Br H Br F F Cl Cl F Cl Br F Cl F Br Br F Br R 32 is (CH 2 ) 2 CH 3 .
  • compounds of Formula 20 are useful process intermediates for preparing compounds of Formulae 17 and 17a as intermediates to compounds of Formula 1, which are useful as component (a) in the present composition.
  • Illustrative of compounds of Formula 20 are those specifically disclosed in Table 4.
  • compounds of Formula 22 are useful process intermediates for preparing compounds of Formulae 17 and 17a as intermediates to compounds of Formula 1, which are useful as component (a) in the present composition.
  • Illustrative of compounds of Formula 22 are those specifically disclosed in Table 5.
  • 2,6-substituted aniline-pyrazole compounds of Formula 1 have now been discovered to have significantly improved pharmacokinetic properties compared to corresponding compounds wherein the phenyl ring connected to R 1 and R 2 has a nonhydrogen substituent at the para position relative to the bond connecting the phenyl ring to the remainder of the molecule.
  • compounds of Formula 1 compared to para-substituted analogs have been found to have a significantly diminished distribution into fat, thereby reducing the possibility of bioaccumulation.
  • 2,6-substituted anilino-pyrazole compounds of Formula 1 wherein R 2 is F have been discovered to retain remarkably high activity when the phenyl para position is unsubstituted against plant fungal diseases, such as caused by Septoria tritici .
  • compounds of Formula 1 are remarkably useful as component (a) in combination with fungicidal compounds of component (b) and optionally other biologically active compounds or agents as component (c) in the present compositions.
  • process intermediates useful for preparing compounds of Formula 1, such as compounds of Formulae 14, 17, 20 and 22 are correspondingly particularly useful.
  • the pharmacokinetic properties of compounds of Formula 1 can be measured using a wide variety of assay protocols known in the science of pharmacology.
  • three male and three female rats receive a single dose of a test substance via oral gavage.
  • Approximately 0.25 mL of blood is collected via tail vein immediately prior to dosing, and then at 0.25, 0.5, 1, 2, 4, 8, 12, 24 h and every 24 h thereafter until sacrifice.
  • fat is also collected to determine the fat:plasma ratio at sacrifice.
  • Blood is collected into tubes that contain ethylenediaminetetracetic acid (EDTA) and centrifuged at 2500 ⁇ g in order to separate plasma from blood cells.
  • EDTA ethylenediaminetetracetic acid
  • the plasma is then extracted by protein precipitation using, for example, acetonitrile and a protein precipitation plate (e.g., Strata Impact Protein Precipitation Plate, part number CEO-7565 of Phenomenex, Torrance, Calif., U.S.A.) following directions provided for the plate.
  • a protein precipitation plate e.g., Strata Impact Protein Precipitation Plate, part number CEO-7565 of Phenomenex, Torrance, Calif., U.S.A.
  • the plasma is extracted just with acetonitrile, vortexed (i.e. mixed using a vortex mixer), and centrifuged to pellet the proteins.
  • the plasma is analyzed for parent compound and/or metabolites by liquid chromatography-mass spectrometry (LC/MS).
  • the fat is homogenized and extracted by an organic solvent such as acetonitrile.
  • the extract is then analyzed for parent compound and/or metabolites by LC/MS.
  • the plasma pharmacokinetic data is then analyzed using nonlinear modeling software (e.g., WinNonlinTM from Pharsight, Cary, N.C., U.S.A.) to determine half-life of the administered compound in plasma, the time after administration when the maximum plasma concentration is reached (T max ), the maximum plasma concentration (C max ) and the area under the plasma concentration curve (AUC).
  • nonlinear modeling software e.g., WinNonlinTM from Pharsight, Cary, N.C., U.S.A.
  • composition comprising (a) at least one compound selected from Formula 1, N-oxides, and salts thereof, with (b) at least one fungicidal compound selected from component (b), component (b) is selected from components (b1) through (b13), i.e. Formulae B1 through B13, respectively, including salts thereof.
  • Component (b1) relates to the compound of Formula B1
  • R b20 and R b21 are independently CH 3 , CF 2 H or CF 3 ; each R b22 is independently halogen or cyano; n is 0, 1, 2 or 3; and L is a direct bond or —CH 2 O— wherein the left bond is connected to the dihydroisoxazole ring and the right bond is connected to the phenyl ring.
  • L is a direct bond or —CH 2 O— wherein the left bond is connected to the dihydroisoxazole ring and the right bond is connected to the phenyl ring.
  • Component (b2) relates to a compound of Formula B2
  • Examples of a compound of Formula B2 include (b2a) (2-chloro-6-fluorophenyl)methyl 2-[1-[2-[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]acetyl]-4-piperidinyl]-4-thiazolecarboxylate (Registry Number 1299409-40-7) and (b2b) (1R)-1,2,3,4-tetrahydro-1-naphthalenyl 2-[1-[2-[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]acetyl]-4-piperidinyl]-4-thiazolecarboxylate (Registry Number 1299409-42-9).
  • Methods for preparing compounds of Formula B2 are described in PCT Patent Publications WO 2009/132785 and WO 2011/051243.
  • Component (b3) relates to a compound of Formula B3
  • Examples of a compound of Formula B3 include (b3a) [[4-methoxy-2-[[[(3S,7R,8R,9S)-9-methyl-8-(2-methyl-1-oxopropoxy)-2,6-dioxo-7-(phenylmethyl)-1,5-dioxonan-3-yl]-amino]carbonyl]-3-pyridinyl]oxy]methyl 2-methylpropanoate (Registry Number 517875-34-2), (b3b) (3S,6S,7R,8R)-3-[[[3-(acetyloxy)-4-methoxy-2-pyridinyl]carbonyl]amino]-6-methyl-4,9-dioxo-8-(phenylmethyl)-1,5-dioxonan-7-yl 2-methylpropanoate (Registry Number 234112-93-7), (b3c) (3S,6S,7R,8R)-3-[[[3-[(
  • Component (b4) relates to a compound of Formula B4
  • R b3 is CH 3 or F.
  • Examples of a compound of Formula B4 include (b4a) 5-fluoro-2-[(4-methylphenyl)-methoxy]-4-pyrimidinamine (Registry Number 1174376-25-0) and (b4b) 5-fluoro-2-[(4-fluorophenyl)methoxy]-4-pyrimidinamine (Registry Number 1174376-11-4).
  • Compounds of Formula B4 can be prepared by methods described in PCT Patent Publication WO 2009/094442.
  • Component (b5) relates to the compound of Formula B5
  • Component (b6) relates to a compound of Formula B6
  • R b4 is —(CH 2 ) 4 CH 3 , —C(CH 3 ) 3 or —(CH 2 ) 2 C ⁇ CH.
  • Examples of a compound of Formula B6 include (b6a) pentyl[6-[[[(Z)-[(1-methyl-1H-tetrazol-5-yl)phenylmethylene]amino]oxy]methyl]-2-pyridinyl]carbamate (Registry Number 500207-05-6), (b6b) 1,1-dimethylethyl N-[6-[[[(Z)-[(1-methyl-1H-tetrazol-5-yl)-phenylmethylene]amino]oxy]methyl]-2-pyridinyl]carbamate (Registry Number 500207-04-5), and (b6c) 3-butyn-1-yl N-[6-[[[(Z)-[(1-methyl-1H-tetrazol-5-yl)phenylmethylene]amino]-oxy]methyl]-2-pyridinyl]carbamate (Registry Number 1202946-82-4).
  • Compounds of Formula B6 can be prepared by methods described
  • Component (b7) relates to the compound of Formula B7
  • Component (b8) relates to the compound of Formula B8
  • Component (b9) relates to a compound of Formula B9
  • R b5 is H or F
  • R b6 is —CF 2 CHFCF 3 or —CF 2 CF 2 H.
  • Examples of a compound of Formula B9 are (b9a) 3-(difluoromethyl)-N-[4-fluoro-2-(1,1,2,3,3,3-hexafluoropropoxy)-phenyl]-1-methyl-1H-pyrazole-4-carboxamide (Registry Number 1172611-40-3) and (b9b) 3-(difluoromethyl)-1-methyl-N-[2-(1,1,2,2-tetrafluoroethoxy)phenyl]-1H-pyrazole-4-carboxamide (Registry Number 923953-98-4).
  • Compounds of Formula B9 can be prepared by methods described in PCT Patent Publication WO 2007/017450.
  • Component (b10) relates to a compound of Formula B10
  • R b8 is H, halogen or C 1 -C 2 alkyl
  • R b9 is C 1 -C 8 alkyl, C 1 -C 8 haloalkyl or C 2 -C 8 alkoxyalkyl
  • R b10 is halogen, C 1 -C 2 alkyl or C 1 -C 2 haloalkyl
  • R b11 is halogen, C 1 -C 2 alkyl or C 1 -C 2 haloalkyl
  • R b12 is C 1 -C 2 alkyl
  • R b13 is H, halogen or C 1 -C 2 alkyl
  • R b14 is C 1 -C 2 alkyl or C 1 -C 2 haloalkyl
  • R b15 is H, C 1 -C 2 alkyl or C 1 -C 2 haloalkyl;
  • W is CH or N
  • Y is CH or N
  • Z is CH or N.
  • Component (b10a) relates to isofetamid (IKF-5411), which is N-[1,1-dimethyl-2-[2-methyl-4-(1-methylethoxy)phenyl]-2-oxoethyl]-3-methyl-2-thiophenecarboxamide (Registry Number 875915-78-9), i.e. the compound of Formula B10a
  • This compound as well as the compounds of Component (b10) can be prepared by methods described in PCT Patent Publications WO 2006/016708 and WO 2007/069777.
  • Component (b10b) relates to tolprocarb (MTF-0301), which is 2,2,2-trifluoroethyl N-[(1S)-2-methyl-1-[[(4-methylbenzoyl)amino]methyl]propyl]carbamate (Registry Number 911499-62-2), i.e. the compound of Formula B10b
  • This compound can be prepared by methods described in US Patent Publication US 2007/0049635 A1.
  • Component (b11) relates to the compound of Formula B11
  • Component (b12) relates to the compound of Formula B12
  • Component (b13) relates to the compound of Formula B13
  • compositions comprising a combination of (a) at least one compound selected from the compounds of Formula 1, including N-oxides and salts thereof, together with (b) at least one fungicidal component selected from Formulae B1 through B13, including salts thereof, described above typically will provide improved control (i.e. prevention and/or cure) of plant disease from synergic contributions of components (a) and (b).
  • the improved plant disease control may be manifest by a broader spectrum or longer duration of plant disease control, or retardation of resistance development.
  • the contributions of components (a) and (b) may be complementarily additive or even greater than additive through synergistic interaction.
  • This invention also relates to a fungicidal composition
  • a fungicidal composition comprising: (a) at least one compound selected from the compounds of Formula 1, (b) at least one fungicidal compound selected from Formulae B1 through B13 described above, and (c) further comprising at least one additional compound or agent that is biologically active.
  • compositions of component (a) with component (b) can be further mixed with (c) one or more other biologically active compounds or agents including insecticides, nematocides, bactericides, acaricides, herbicides, herbicide safeners, growth regulators such as insect molting inhibitors and rooting stimulants, chemosterilants, semiochemicals, repellents, attractants, pheromones, feeding stimulants, plant nutrients, other biologically active compounds or entomopathogenic bacteria, virus or fungi to form a multi-component pesticide giving an even broader spectrum of agricultural protection.
  • General references for these agricultural protectants include The Pesticide Manual, 13th Edition, C. D. S.
  • component (c) comprises at least one additional compound that is a fungicide (i.e. an additional fungicidal compound).
  • additional fungicidal compounds in component (c) are typically selected from the group consisting of (c1) methyl benzimidazole carbamate (MBC) fungicides; (c2) dicarboximide fungicides; (c3) demethylation inhibitor (DMI) fungicides; (c4) phenylamide fungicides; (c5) amine/morpholine fungicides; (c6) phospholipid biosynthesis inhibitor fungicides; (c7) carboxamide fungicides; (c8) hydroxy(2-amino-)pyrimidine fungicides; (c9) anilinopyrimidine fungicides; (c10) N-phenyl carbamate fungicides; (c11) quinone outside inhibitor (QoI) fungicides; (c12) phenyl
  • component (c) comprises at least one fungicidal compound from each of two different groups selected from (c1) through (c46).
  • Methyl benzimidazole carbamate (MBC) fungicides (c1) (FRAC (Fungicide Resistance Action Committee) code 1) inhibit mitosis by binding to 3-tubulin during microtubule assembly. Inhibition of microtubule assembly can disrupt cell division, transport within the cell and cell structure.
  • Methyl benzimidazole carbamate fungicides include benzimidazole and thiophanate fungicides.
  • the benzimidazoles include benomyl, carbendazim, fuberidazole and thiabendazole.
  • the thiophanates include thiophanate and thiophanate-methyl.
  • “Dicarboximide fungicides (c2)” FRAC code 2 are proposed to inhibit a lipid peroxidation in fungi through interference with NADH cytochrome c reductase. Examples include chlozolinate, iprodione, procymidone and vinclozolin.
  • DMI Demethylation inhibitor fungicides
  • FRAC code 3 “Demethylation inhibitor (DMI) fungicides
  • Sterols such as ergosterol, are needed for membrane structure and function, making them essential for the development of functional cell walls. Therefore, exposure to these fungicides result in abnormal growth and eventually death of sensitive fungi.
  • DMI fungicides are divided between several chemical classes: azoles (including triazoles and imidazoles), pyrimidines, piperazines and pyridines.
  • the triazoles include azaconazole, bitertanol, bromuconazole, cyproconazole, difenoconazole, diniconazole (including diniconazole-M), epoxiconazole, etaconazole, fenbuconazole, fluquinconazole, flusilazole, flutriafol, hexaconazole, imibenconazole, ipconazole, metconazole, myclobutanil, penconazole, propiconazole, prothioconazole, quinconazole, simeconazole, tebuconazole, tetraconazole, triadimefon, triadimenol, triticonazole and uniconazole.
  • the imidazoles include clotrimazole, econazole, imazalil, isoconazole, miconazole, oxpoconazole, prochloraz, pefurazoate and triflumizole.
  • the pyrimidines include fenarimol, nuarimol and triarimol.
  • the piperazines include triforine.
  • the pyridines include buthiobate and pyrifenox. Biochemical investigations have shown that all of the above mentioned fungicides are DMI fungicides as described by K. H. Kuck et al. in Modern Selective Fungicides—Properties, Applications and Mechanisms of Action , H. Lyr (Ed.), Gustav Fischer Verlag: New York, 1995, 205-258.
  • Phenylamide fungicides (c4) are specific inhibitors of RNA polymerase in Oomycete fungi. Sensitive fungi exposed to these fungicides show a reduced capacity to incorporate uridine into rRNA. Growth and development in sensitive fungi is prevented by exposure to this class of fungicide.
  • Phenylamide fungicides include acylalanine, oxazolidinone and butyrolactone fungicides.
  • the acylalanines include benalaxyl, benalaxyl-M, furalaxyl, metalaxyl, metalaxyl-M (also known as mefenoxam).
  • the oxazolidinones include oxadixyl.
  • the butyrolactones include ofurace.
  • Amine/morpholine fungicides (also known as non-DMI sterol biosynthesis inhibitors) include morpholine, piperidine and spiroketal-amine fungicides.
  • the morpholines include aldimorph, dodemorph, fenpropimorph, tridemorph and trimorphamide.
  • the piperidines include fenpropidin and piperalin.
  • the spiroketal-amines include spiroxamine.
  • Phospholipid biosynthesis inhibitor fungicides (c6) (FRAC code 6) inhibit growth of fungi by affecting phospholipid biosynthesis.
  • Phospholipid biosynthesis fungicides include phosphorothiolate and dithiolane fungicides.
  • the phosphorothiolates include edifenphos, iprobenfos and pyrazophos.
  • the dithiolanes include isoprothiolane.
  • Carboxamide fungicides (c7) inhibit Complex II (succinate dehydrogenase) fungal respiration by disrupting a key enzyme in the Krebs Cycle (TCA cycle) named succinate dehydrogenase Inhibiting respiration prevents the fungus from making ATP, and thus inhibits growth and reproduction.
  • Carboxamide fungicides include benzamide, furan carboxamide, oxathiin carboxamide, thiazole carboxamide, pyrazole carboxamide and pyridine carboxamide.
  • the benzamides include benodanil, flutolanil and mepronil.
  • the furan carboxamides include fenfuram.
  • the oxathiin carboxamides include carboxin and oxycarboxin.
  • the thiazole carboxamides include thifluzamide.
  • the pyrazole carboxamides include bixafen, furametpyr, isopyrazam, fluxapyroxad, penthiopyrad, sedaxane (N-[2-(1S,2R)-[1,1′-bicyclopropyl]-2-ylphenyl]-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxamide) and penflufen (N-[2-(1,3-dimethylbutyl)phenyl]-5-fluoro-1,3-dimethyl-1H-pyrazole-4-carboxamide) (PCT Patent Publication WO 2003/010149).
  • the pyridine carboxamides include boscalid.
  • Haldroxy(2-amino-)pyrimidine fungicides (c8) inhibit nucleic acid synthesis by interfering with adenosine deaminase. Examples include bupirimate, dimethirimol and ethirimol.
  • “Anilinopyrimidine fungicides (c9)” (FRAC code 9) are proposed to inhibit biosynthesis of the amino acid methionine and to disrupt the secretion of hydrolytic enzymes that lyse plant cells during infection. Examples include cyprodinil, mepanipyrim and pyrimethanil.
  • N-Phenyl carbamate fungicides (c10)” (FRAC code 10) inhibit mitosis by binding to ⁇ -tubulin and disrupting microtubule assembly. Inhibition of microtubule assembly can disrupt cell division, transport within the cell and cell structure. Examples include diethofencarb.
  • QoI Quinone outside inhibitor
  • fungicides c11
  • FRAC code 11 inhibit Complex III mitochondrial respiration in fungi by affecting ubiquinol oxidase. Oxidation of ubiquinol is blocked at the “quinone outside” (Q o ) site of the cytochrome bc 1 complex, which is located in the inner mitochondrial membrane of fungi Inhibiting mitochondrial respiration prevents normal fungal growth and development.
  • Quinone outside inhibitor fungicides include methoxyacrylate, methoxycarbamate, oximinoacetate, oximinoacetamide and dihydrodioxazine fungicides (collectively also known as strobilurin fungicides), and oxazolidinedione, imidazolinone and benzylcarbamate fungicides.
  • the methoxyacrylates include azoxystrobin, enestroburin (SYP-Z071) and picoxystrobin.
  • the methoxycarbamates include pyraclostrobin and pyrametostrobin.
  • the oximinoacetates include kresoxim-methyl, pyraoxystrobin and trifloxystrobin.
  • the oximinoacetamides include dimoxystrobin, metominostrobin, orysastrobin and ⁇ -(methoxyimino)-N-methyl-2-[[[1-[3-(trifluoro-methyl)phenyl]ethoxy]imino]methyl]benzeneacetamide.
  • the dihydrodioxazines include fluoxastrobin.
  • the oxazolidinediones include famoxadone.
  • the imidazolinones include fenamidone.
  • the benzylcarbamates include pyribencarb.
  • Phenylpyrrole fungicides (c12) inhibit a MAP protein kinase associated with osmotic signal transduction in fungi.
  • Fenpiclonil and fludioxonil are examples of this fungicide class.
  • Quinoline fungicides (c13) are proposed to inhibit signal transduction by affecting G-proteins in early cell signaling. They have been shown to interfere with germination and/or appressorium formation in fungi that cause powdery mildew diseases. Quinoxyfen is an example of this class of fungicide.
  • Lipid peroxidation inhibitor fungicides (c14) are proposed to inhibit lipid peroxidation which affects membrane synthesis in fungi. Members of this class, such as etridiazole, may also affect other biological processes such as respiration and melanin biosynthesis.
  • Lipid peroxidation fungicides include aromatic carbon and 1,2,4-thiadiazole fungicides.
  • the aromatic carbons include biphenyl, chloroneb, dicloran, quintozene, tecnazene and tolclofos-methyl.
  • the 1,2,4-thiadiazoles include etridiazole.
  • Melanin biosynthesis inhibitors-reductase (MBI-R) fungicides (c15) inhibit the naphthal reduction step in melanin biosynthesis.
  • Melanin is required for host plant infection by some fungi.
  • Melanin biosynthesis inhibitors-reductase fungicides include isobenzofuranone, pyrroloquinolinone and triazolobenzothiazole fungicides.
  • the isobenzofuranones include fthalide.
  • the pyrroloquinolinones include pyroquilon.
  • the triazolobenzothiazoles include tricyclazole.
  • Melanin biosynthesis inhibitors-dehydratase (MBI-D) fungicides (c16) inhibit scytalone dehydratase in melanin biosynthesis.
  • Melanin in required for host plant infection by some fungi.
  • Melanin biosynthesis inhibitors-dehydratase fungicides include cyclopropanecarboxamide, carboxamide and propionamide fungicides.
  • the cyclopropanecarboxamides include carpropamid.
  • the carboxamides include diclocymet.
  • the propionamides include fenoxanil.
  • Haldroxyanilide fungicides (c17) inhibit C4-demethylase which plays a role in sterol production. Examples include fenhexamid.
  • Squalene-epoxidase inhibitor fungicides (c18) (FRAC code 18) inhibit squalene-epoxidase in ergosterol biosynthesis pathway.
  • Sterols such as ergosterol are needed for membrane structure and function, making them essential for the development of functional cell walls. Therefore exposure to these fungicides result in abnormal growth and eventually death of sensitive fungi.
  • Squalene-epoxidase inhibitor fungicides include thiocarbamate and allylamine fungicides.
  • the thiocarbamates include pyributicarb.
  • the allylamines include naftifine and terbinafine.
  • Polyoxin fungicides (c19)” (FRAC code 19) inhibit chitin synthase. Examples include polyoxin.
  • Phenylurea fungicides (c20) are proposed to affect cell division. Examples include pencycuron.
  • Quinone inside inhibitor (QiI) fungicides (c21) inhibit Complex III mitochondrial respiration in fungi by affecting ubiquinol reductase. Reduction of ubiquinol is blocked at the “quinone inside” (Q i ) site of the cytochrome bc 1 complex, which is located in the inner mitochondrial membrane of fungi. Inhibiting mitochondrial respiration prevents normal fungal growth and development.
  • Quinone inside inhibitor fungicides include cyanoimidazole and sulfamoyltriazole fungicides.
  • the cyanoimidazoles include cyazofamid.
  • the sulfamoyltriazoles include amisulbrom.
  • Benzamide fungicides (c22) inhibit mitosis by binding to 3-tubulin and disrupting microtubule assembly Inhibition of microtubule assembly can disrupt cell division, transport within the cell and cell structure. Examples include zoxamide.
  • Enopyranuronic acid antibiotic fungicides (c23)
  • FRAC code 23 inhibit growth of fungi by affecting protein biosynthesis. Examples include blasticidin-S.
  • Halopyranosyl antibiotic fungicides (c24)” (FRAC code 24) inhibit growth of fungi by affecting protein biosynthesis. Examples include kasugamycin.
  • Glucopyranosyl antibiotic protein synthesis fungicides (c25)
  • FRAC code 25 inhibit growth of fungi by affecting protein biosynthesis. Examples include streptomycin.
  • Glucopyranosyl antibiotic trehalase and inositol biosynthesis fungicides (c26)” (FRAC code 26) inhibit trehalase in inositol biosynthesis pathway. Examples include validamycin.
  • “Cyanoacetamideoxime fungicides (c27)” include cymoxanil.
  • “Carbamate fungicides (c28)” (FRAC code 28) are considered multi-site inhibitors of fungal growth. They are proposed to interfere with the synthesis of fatty acids in cell membranes, which then disrupts cell membrane permeability. Propamacarb, iodocarb, and prothiocarb are examples of this fungicide class.
  • Oxidative phosphorylation uncoupling fungicides (c29)” (FRAC code 29) inhibit fungal respiration by uncoupling oxidative phosphorylation Inhibiting respiration prevents normal fungal growth and development.
  • This class includes 2,6-dinitroanilines such as fluazinam, pyrimidonehydrazones such as ferimzone and dinitrophenyl crotonates such as dinocap, meptyldinocap and binapacryl.
  • Organic tin fungicides (c30) (FRAC code 30) inhibit adenosine triphosphate (ATP) synthase in oxidative phosphorylation pathway.
  • examples include fentin acetate, fentin chloride and fentin hydroxide.
  • Carboxylic acid fungicides (c31) inhibit growth of fungi by affecting deoxyribonucleic acid (DNA) topoisomerase type II (gyrase). Examples include oxolinic acid.
  • Heteroaromatic fungicides (c32) are proposed to affect DNA/ribonucleic acid (RNA) synthesis.
  • Heteroaromatic fungicides include isoxazole and isothiazolone fungicides.
  • the isoxazoles include hymexazole and the isothiazolones include octhilinone.
  • Phosphonate fungicides include phosphorous acid and its various salts, including fosetyl-aluminum.
  • Phthalamic acid fungicides (c34) include teclofthalam.
  • Benzotriazine fungicides (c35) include triazoxide.
  • Benzene-sulfonamide fungicides (c36) include flusulfamide.
  • “Pyridazinone fungicides (c37)” include diclomezine.
  • Thiophene-carboxamide fungicides (c38) are proposed to affect ATP production. Examples include silthiofam.
  • “Pyrimidinamide fungicides (c39)” (FRAC code 39) inhibit growth of fungi by affecting phospholipid biosynthesis and include diflumetorim.
  • Carboxylic acid amide (CAA) fungicides (c40) are proposed to inhibit phospholipid biosynthesis and cell wall deposition. Inhibition of these processes prevents growth and leads to death of the target fungus.
  • Carboxylic acid amide fungicides include cinnamic acid amide, valinamide carbamate and mandelic acid amide fungicides.
  • the cinnamic acid amides include dimethomorph and flumorph.
  • the valinamide carbamates include benthiavalicarb, benthiavalicarb-isopropyl, iprovalicarb and valifenalate (valiphenal).
  • the mandelic acid amides include mandipropamid, N-[2-[4-[[3-(4-chlorophenyl)-2-propyn-1-yl]oxy]-3-methoxyphenyl]ethyl]-3-methyl-2-[(methylsulfonyl)-amino]butanamide and N-[2-[4-[[3-(4-chlorophenyl)-2-propyn-1-yl]oxy]-3-methoxyphenyl]-ethyl]-3-methyl-2-[(ethylsulfonyl)amino]butanamide.
  • Tetracycline antibiotic fungicides (c41) (FRAC code 41) inhibit growth of fungi by affecting complex 1 nicotinamide adenine dinucleotide (NADH) oxidoreductase. Examples include oxytetracycline.
  • Thiocarbamate fungicides (c42) include methasulfocarb.
  • Benzamide fungicides (c43) inhibit growth of fungi by delocalization of spectrin-like proteins.
  • examples include acylpicolide fungicides such as fluopicolide and fluopyram.
  • Host plant defense induction fungicides include benzo-thiadiazole, benzisothiazole and thiadiazole-carboxamide fungicides.
  • the benzo-thiadiazoles include acibenzolar-S-methyl.
  • the benzisothiazoles include probenazole.
  • the thiadiazole-carboxamides include tiadinil and isotianil.
  • Multi-site contact fungicides (c45)” inhibit fungal growth through multiple sites of action and have contact/preventive activity.
  • This class of fungicides includes: “copper fungicides (c45.1) (FRAC code M1)”, “sulfur fungicides (c45.2) (FRAC code M2)”, “dithiocarbamate fungicides (c45.3) (FRAC code M3)”, “phthalimide fungicides (c45.4) (FRAC code M4)”, “chloronitrile fungicides (c45.5) (FRAC code M5)”, “sulfamide fungicides (c45.6) (FRAC code M6)”, “guanidine fungicides (c45.7) (FRAC code M7)” “triazine fungicides (c45.8) (FRAC code M8)” and “quinone fungicides (c45.9) (FRAC code M9)”.
  • Copper fungicides are inorganic compounds containing copper, typically in the copper(II) oxidation state; examples include copper oxychloride, copper sulfate and copper hydroxide, including compositions such as Bordeaux mixture (tribasic copper sulfate).
  • Sulfur fungicides are inorganic chemicals containing rings or chains of sulfur atoms; examples include elemental sulfur.
  • Dithiocarbamate fungicides contain a dithiocarbamate molecular moiety; examples include mancozeb, metiram, propineb, ferbam, maneb, thiram, zineb and ziram.
  • Phthalimide fungicides contain a phthalimide molecular moiety; examples include folpet, captan and captafol. “Chloronitrile fungicides” contain an aromatic ring substituted with chloro and cyano; examples include chlorothalonil. “Sulfamide fungicides” include dichlofluanid and tolylfluanid. “Guanidine fungicides” include dodine, guazatine and iminoctadine. “Triazine fungicides” include anilazine. “Quinone fungicides” include dithianon.
  • “Fungicides other than fungicides of component (a) and components (c1) through (c45); (c46)” include certain fungicides whose mode of action may be unknown. These include: (c46.1) “thiazole carboxamide fungicides” (FRAC code U5), (c46.2) “phenyl-acetamide fungicides” (FRAC code U6), (c46.3) “quinazolinone fungicides” (FRAC code U7), (c46.4) “benzophenone fungicides” (FRAC code U8) and (c46.5) “triazolopyrimidylamine fungicides” (FRAC code 45).
  • the thiazole carboxamides include ethaboxam.
  • the phenyl-acetamides include cyflufenamid and N-[[(cyclopropyl-methoxy)amino][6-(difluoromethoxy)-2,3-difluorophenyl]-methylene]benzeneacetamide.
  • the quinazolinones include proquinazid and 2-butoxy-6-iodo-3-propyl-4H-1-benzopyran-4-one.
  • the benzophenones include metrafenone and pyriofenone.
  • the triazolopyrimidylamines include ametoctradin and are believed to inhibit Complex III mitochondrial respiration by binding to an unelucidated site on ubiquinone-cytochrome bc1 reductase.
  • the (c46) class also includes bethoxazin, neo-asozin (ferric methanearsonate), fenpyrazamine, pyrrolnitrin, quinomethionate, tebufloquin, 2-[[2-fluoro-5-(trifluoromethyl)phenyl]thio]-2-[3-(2-methoxyphenyl)-2-thiazolidinylidene]acetonitrile, 3-[5-(4-chlorophenyl)-2,3-dimethyl-3-isoxazolidinyl]pyridine, 4-fluorophenyl N-[1-[[[1-(4-cyanophenyl)ethyl]sulfonyl]methyl]
  • “Fungicides other than fungicides of component (a) and components (c1) through (c45); (c46)” also include (c46.5) 6-quinolinyloxyacetamide compounds of Formula C1 and salts thereof
  • “Fungicides other than fungicides of component (a) and components (c1) through (c45); (c46)” also include (c46.6) N′-[4-[[3-[(4-chlorophenyl)methyl]-1,2,4-thiadiazol-5-yl]oxy]-2,5-dimethylphenyl]-N-ethyl-N-methylmethanimidamide, which is believed to inhibit C24-methyl transferase involved in biosynthesis of sterols.
  • component (c) fungicidal compounds examples include those listed in Embodiment 31, more particularly Embodiment 32, and even more particularly Embodiment 33.
  • Compositions comprising a combination of (a) at least one compound selected from the compounds of Formula 1, including N-oxides and salts thereof, (b) at least one fungicidal component selected from Formulae B1 through B13, including salts thereof and (c) at least one additional fungicidal compound (e.g., (c1) through (c46) of Embodiment 30, including the corresponding fungicidal compounds described above) can provide improved control (i.e. prevention and/or cure) of plant disease from synergic contributions of components (a), (b) and (c).
  • the improved plant disease control may be manifest by a broader spectrum or longer duration of plant disease control, or retardation of resistance development.
  • the contributions of components (a), (b) and (c) may be complementarily additive or even greater than additive through synergistic interaction. Addition of component (c) may provide stronger synergy than resulting from combination of components (a) and (b).
  • a fungicidal composition comprising (a) at least one compound selected from the compounds of Formula 1, including N-oxides and salts thereof, (b) at least one fungicidal compound selected from Formulae B1 through B13 including salts thereof, described above, and (c) further comprising at least one additional compound or agent that is biologically active, besides the fungicidal compounds (c1) through (c46) described above, component (c) can also be selected from compounds or agents having biological activity that is other than fungicidal.
  • insecticides such as abamectin, acephate, acetamiprid, acetoprole, acrinathrin, aldicarb, amidoflumet, amitraz, avermectin, azadirachtin, azinphos-methyl, bifenthrin, bifenazate, bistrifluron, buprofezin, carbofuran, cartap, chinomethionat, chlorfenapyr, chlorfluazuron, chlorantraniliprole, chlorpyrifos, chlorpyrifos-methyl, chlorobenzilate, chromafenozide, clothianidin, cyantraniliprole, cyflumetofen, cyfluthrin, beta-cyfluthrin, cyhalothrin
  • Bacillus thuringiensis subsp. kurstaki , and the encapsulated delta-endotoxins of Bacillus thuringiensis (e.g., Cellcap, MPV, MPVII); entomopathogenic fungi, such as green muscardine fungus; and entomopathogenic virus including baculovirus, nucleopolyhedro virus (NPV) such as HzNPV, AfNPV; and granulosis virus (GV) such as CpGV.
  • NPV nucleopolyhedro virus
  • GV granulosis virus
  • composition of the present invention which comprises, in addition to a components (a) and (b), at least one invertebrate pest control compound or agent selected from the group consisting of abamectin, acephate, acetamiprid, acetoprole, acrinathrin, aldicarb, amidoflumet, amitraz, avermectin, azadirachtin, azinphos-methyl, bifenthrin, bifenazate, bistrifluron, buprofezin, carbofuran, cartap, chinomethionat, chlorfenapyr, chlorfluazuron, chlorantraniliprole, chlorpyrifos, chlorpyrifos-methyl, chlorobenzilate, chromafenozide, clothianidin, cyantraniliprole, cyflumetofen, cyfluthrin, beta-cyfluthrin, cyhaloth
  • combinations of a mixture of components (a) and (b) fungicidal compounds with invertebrate pest control compounds or agents can result in a greater-than-additive (i.e. synergistic) effect. Reducing the quantity of active ingredients released in the environment while ensuring effective pest control is always desirable.
  • synergism of invertebrate pest control active ingredients occurs at application rates giving agronomically satisfactory levels of invertebrate pest control, such combinations can be advantageous for reducing crop production cost and decreasing environmental load. Synergism can also result in increased plant disease control or protection.
  • component (a) i.e. at least one compound selected from compounds of Formula 1, N-oxides, and salts thereof
  • component (b) are present in fungicidally effective amounts.
  • the weight ratio of component (a) to component (b) i.e. one or more additional fungicidal compounds
  • compositions where in the weight ratio of component (a) to component (b) is from about 125:1 to about 1:125. With many fungicidal compounds of component (b), these compositions are particularly effective for controlling plant diseases caused by fungal plant pathogens.
  • compositions wherein the weight ratio of component (a) to component (b) is from about 25:1 to about 1:25, or from about 5:1 to about 1:5.
  • weight ratios and application rates of fungicidal compounds necessary for the desired spectrum of fungicidal protection and control.
  • Table A1 lists specific combinations of a Component (b) compound with Compound 1 as Component (a) illustrative of the mixtures, compositions and methods of the present invention. (Compound numbers refer to compounds in Index Table A.)
  • the second column of Table A1 lists the specific Component (b) compound (e.g., “1-[4-[4-[5-(2,6-difluorophenyl)-4,5-dihydro-3-isoxazolyl]-2-thiazolyl]-1-piperidinyl]-2-[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]ethanone (b1a)” in the first line).
  • the third, fourth and fifth columns of Table A1 lists ranges of weight ratios for rates at which the Component (a) compound is typically applied to a field-grown crop relative to Component (b).
  • the first line of Table A1 specifically discloses the combination of Compound 1 with Component (b1a) is typically applied in a weight ratio of Compound 1 to Component (b1a) of between 400:1 and 1:1.
  • the remaining lines of Table A1 are to be construed similarly.
  • Tables A2 through A13 are each constructed the same as Table A1 above except that entries below the “Component (a)” column heading are replaced with the respective Component (a) Column Entry shown below.
  • Table A2 the entries below the “Component (a)” column heading all recite “Compound 2”, and the first line below the column headings in Table A2 specifically discloses combination of Compound 2 with 1-[4-[4-[5-(2,6-difluorophenyl)-4,5-dihydro-3-isoxazolyl]-2-thiazolyl]-1-piperidinyl]-2-[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]ethanone.
  • Tables A3 through A13 are constructed similarly.
  • Tables B1 through B13 Specific mixtures are listed in Tables B1 through B13.
  • Component numbers refer to compounds in Index Table A, and Component (b) is identified in Table A1.
  • Table B1 each line below the column headings “Component (a)” and “Component (b)” specifically discloses a mixture of Component (a), which is Compound 1, with a Component (b) fungicidal compound.
  • the entries under the heading “Illustrative Ratios” disclose seven specific weight ratios of Component (a) relative to Component (b) for the disclosed mixture.
  • the first line of Table B1 discloses a mixture of Compound 1 with 1-[4-[4-[5-(2,6-difluorophenyl)-4,5-dihydro-3-isoxazolyl]-2-thiazolyl]-1-piperidinyl]-2-[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]ethanone (b1) and lists weight ratios of Compound 1 relative to Component (b1) of 2:1, 4:1, 8:1, 20:1, 50:1, 100:1 or 200:1. Table B1 thus supplements with specific ratios the general ranges of ratios for the combinations disclosed in Table A1.
  • Tables B2 through B13 are each constructed the same as Table B1 above except that entries below the “Component (a)” column heading are replaced with the respective Component (a) Column Entry shown below.
  • Table B2 the entries below the “Component (a)” column heading all recite “Compound 2”, and the first line below the column headings in Table A2 specifically discloses a mixture of Compound 2 with 1-[4-[4-[5-(2,6-difluorophenyl)-4,5-dihydro-3-isoxazolyl]-2-thiazolyl]-1-piperidinyl]-2-[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]ethanone.
  • Tables B3 through B13 are constructed similarly. Tables B2 through B13 thus supplement with specific ratios the general ranges of ratios for the combinations disclosed in Tables A2 through A13, respectively.
  • the present invention includes embodiments wherein the composition comprising components (a) and (b) further comprises as component (c) one or more biologically active compounds or agents. Therefore embodiments of the present composition include combinations of the mixtures disclosed in Tables A1 through A12 and B1 through B13 with additional biological compounds or agents. Of note as additional biological compounds or agents are fungicidal compounds selected from (c1) through (c46) already described.
  • the weight ratio of component (c) to component (a) is generally between about 1:3000 and about 3000:1, more typically between about 1:500 and about 500:1, between about 125:1 and about 1:125, and between about 25:1 and 1:25 and most typically between about 5:1 and about 1:5.
  • One skilled in the art can easily determine through simple experimentation the weight ratios and application rates of fungicidal compounds necessary for the desired spectrum of plant disease protection and control.
  • Table C lists typical, more typical, and most typical weight ratios for specific component (c) fungicides relative to component (a) in compositions comprising components (a) and (c) either before (i.e. without component (b)) or after inclusion of component (b).
  • Table C The particular weight ratios defining the weight ratio ranges in Table C constitute disclosure of specific weight ratios. Table C also specifically discloses an additional illustrative weight ratio. Illustrative of specific combinations of components (a), (b) and (c) in the compositions of the present invention are specific combinations and weight ratios of components (a) and (b) listed in Tables B1 through B13 further combined with particular component (c) fungicidal compounds in the specific weight ratios disclosed in Table C.
  • a compound selected from compounds of Formula 1, N-oxides, and salts thereof, or a mixture (i.e. composition) comprising the compound with (b) at least one fungicidal compound selected from (b1) through (b13) and salts thereof as described in the Summary of the Invention, will generally be used to provide fungicidal active ingredients in further compositions, i.e. formulations, with at least one additional component selected from the group consisting of surfactants, solid diluents and liquid diluents, which serves as a carrier.
  • the formulation or composition ingredients are selected to be consistent with the physical properties of the active ingredients, mode of application and environmental factors such as soil type, moisture and temperature.
  • component (a) i.e. at least one compound of Formula 1, N-oxides, or salts thereof
  • component (b) e.g., selected from (b1) to (b13) and salts thereof as described above
  • one or more other biologically active compounds or agents i.e. insecticides, other fungicides, nematocides, acaricides, herbicides and other biological agents
  • insecticides, other fungicides, nematocides, acaricides, herbicides and other biological agents can be formulated in a number of ways, including:
  • Liquid compositions include solutions (including emulsifiable concentrates), suspensions, emulsions (including microemulsions and/or suspoemulsions) and the like, which optionally can be thickened into gels.
  • aqueous liquid compositions are soluble concentrate, suspension concentrate, capsule suspension, concentrated emulsion, microemulsion and suspo-emulsion.
  • nonaqueous liquid compositions are emulsifiable concentrate, microemulsifiable concentrate, dispersible concentrate and oil dispersion.
  • the general types of solid compositions are dusts, powders, granules, pellets, prills, pastilles, tablets, filled films (including seed coatings) and the like, which can be water-dispersible (“wettable”) or water-soluble. Films and coatings formed from film-forming solutions or flowable suspensions are particularly useful for seed treatment.
  • Active ingredient can be (micro)encapsulated and further formed into a suspension or solid formulation; alternatively the entire formulation of active ingredient can be encapsulated (or “overcoated”). Encapsulation can control or delay release of the active ingredient.
  • An emulsifiable granule combines the advantages of both an emulsifiable concentrate formulation and a dry granular formulation. High-strength compositions are primarily used as intermediates for further formulation.
  • composition embodiment wherein granules of a solid composition comprising a compound of Formula 1 (or an N-oxide or salt thereof) is mixed with granules of a solid composition comprising component (b). These mixtures can be further mixed with granules comprising one or more additional biologically active compounds or agents, e.g., additional agricultural protectants.
  • two or more agricultural protectants e.g., a component (a) (Formula 1) compound, a component (b) compound, (c) an agricultural protectant other than component (a) or (b)
  • granule mixtures can be in accordance with the general granule mixture disclosure of PCT Patent Publication WO 94/24861 or more preferably the homogeneous granule mixture teaching of U.S. Pat. No. 6,022,552.
  • Sprayable formulations are typically extended in a suitable medium before spraying. Such liquid and solid formulations are formulated to be readily diluted in the spray medium, usually water. Spray volumes can range from about from about one to several thousand liters per hectare, but more typically are in the range from about ten to several hundred liters per hectare. Sprayable formulations can be tank mixed with water or another suitable medium for foliar treatment by aerial or ground application, or for application to the growing medium of the plant. Liquid and dry formulations can be metered directly into drip irrigation systems or metered into the furrow during planting. Liquid and solid formulations can be applied onto seeds of crops and other desirable vegetation as seed treatments before planting to protect developing roots and other subterranean plant parts and/or foliage through systemic uptake.
  • the formulations will typically contain effective amounts of active ingredient, diluent and surfactant within the following approximate ranges which add up to 100 percent by weight.
  • Weight Percent Active Ingredient Diluent Surfactant Water-Dispersible and Water- 0.001-90 0-99.999 0-15 soluble Granules, Tablets and Powders Oil Dispersions, Suspensions, 1-50 40-99 0-50 Emulsions, Solutions (including Emulsifiable Concentrates) Dusts 1-25 70-99 0-5 Granules and Pellets 0.001-99 5-99.999 0-15 High Strength Compositions 90-99 0-10 0-2
  • Solid diluents include, for example, clays such as bentonite, montmorillonite, attapulgite and kaolin, gypsum, cellulose, titanium dioxide, zinc oxide, starch, dextrin, sugars (e.g., lactose, sucrose), silica, talc, mica, diatomaceous earth, urea, calcium carbonate, sodium carbonate and bicarbonate, and sodium sulfate.
  • Typical solid diluents are described in Watkins et al., Handbook of Insecticide Dust Diluents and Carriers, 2nd Ed., Dorland Books, Caldwell, N.J.
  • Liquid diluents include, for example, water, N,N-dimethylalkanamides (e.g., N,N-dimethylformamide), limonene, dimethyl sulfoxide, N-alkylpyrrolidones (e.g., N-methylpyrrolidinone), ethylene glycol, triethylene glycol, propylene glycol, dipropylene glycol, polypropylene glycol, propylene carbonate, butylene carbonate, paraffins (e.g., white mineral oils, normal paraffins, isoparaffins), alkylbenzenes, alkylnaphthalenes, glycerine, glycerol triacetate, sorbitol, triacetin, aromatic hydrocarbons, dearomatized aliphatics, alkylbenzenes, alkylnaphthalenes, ketones such as cyclohexanone, 2-heptanone, isophorone and 4-hydroxy-4-methyl
  • Liquid diluents also include glycerol esters of saturated and unsaturated fatty acids (typically C 6 -C 22 ), such as plant seed and fruit oils (e.g., oils of olive, castor, linseed, sesame, corn (maize), peanut, sunflower, grapeseed, safflower, cottonseed, soybean, rapeseed, coconut and palm kernel), animal-sourced fats (e.g., beef tallow, pork tallow, lard, cod liver oil, fish oil), and mixtures thereof.
  • plant seed and fruit oils e.g., oils of olive, castor, linseed, sesame, corn (maize), peanut, sunflower, grapeseed, safflower, cottonseed, soybean, rapeseed, coconut and palm kernel
  • animal-sourced fats e.g., beef tallow, pork tallow, lard, cod liver oil, fish oil
  • Liquid diluents also include alkylated fatty acids (e.g., methylated, ethylated, butylated) wherein the fatty acids may be obtained by hydrolysis of glycerol esters from plant and animal sources, and can be purified by distillation.
  • alkylated fatty acids e.g., methylated, ethylated, butylated
  • Typical liquid diluents are described in Marsden, Solvents Guide, 2nd Ed., Interscience, New York, 1950.
  • the solid and liquid compositions of the present invention often include one or more surfactants.
  • surfactants also known as “surface-active agents”
  • surface-active agents generally modify, most often reduce, the surface tension of the liquid.
  • surfactants can be useful as wetting agents, dispersants, emulsifiers or defoaming agents.
  • Nonionic surfactants useful for the present compositions include, but are not limited to: alcohol alkoxylates such as alcohol alkoxylates based on natural and synthetic alcohols (which may be branched or linear) and prepared from the alcohols and ethylene oxide, propylene oxide, butylene oxide or mixtures thereof; amine ethoxylates, alkanolamides and ethoxylated alkanolamides; alkoxylated triglycerides such as ethoxylated soybean, castor and rapeseed oils; alkylphenol alkoxylates such as octylphenol ethoxylates, nonylphenol ethoxylates, dinonyl phenol ethoxylates and dodecyl phenol ethoxylates (prepared from the phenols and ethylene oxide, propylene oxide, butylene oxide or mixtures thereof); block polymers prepared from ethylene oxide or propylene
  • Useful anionic surfactants include, but are not limited to: alkylaryl sulfonic acids and their salts; carboxylated alcohol or alkylphenol ethoxylates; diphenyl sulfonate derivatives; lignin and lignin derivatives such as lignosulfonates; maleic or succinic acids or their anhydrides; olefin sulfonates; phosphate esters such as phosphate esters of alcohol alkoxylates, phosphate esters of alkylphenol alkoxylates and phosphate esters of styryl phenol ethoxylates; protein-based surfactants; sarcosine derivatives; styryl phenol ether sulfate; sulfates and sulfonates of oils and fatty acids; sulfates and sulfonates of ethoxylated alkylphenols; sulfates of alcohols; sulfates of e
  • Useful cationic surfactants include, but are not limited to: amides and ethoxylated amides; amines such as N-alkyl propanediamines, tripropylenetriamines and dipropylenetetramines, and ethoxylated amines, ethoxylated diamines and propoxylated amines (prepared from the amines and ethylene oxide, propylene oxide, butylene oxide or mixtures thereof); amine salts such as amine acetates and diamine salts; quaternary ammonium salts such as quaternary salts, ethoxylated quaternary salts and diquaternary salts; and amine oxides such as alkyldimethylamine oxides and bis-(2-hydroxyethyl)-alkylamine oxides.
  • amines such as N-alkyl propanediamines, tripropylenetriamines and dipropylenetetramines, and ethoxylated amine
  • Nonionic, anionic and cationic surfactants and their recommended uses are disclosed in a variety of published references including McCutcheon's Emulsifiers and Detergents , annual American and International Editions published by McCutcheon's Division, The Manufacturing Confectioner Publishing Co.; Sisely and Wood, Encyclopedia of Surface Active Agents , Chemical Publ. Co., Inc., New York, 1964; and A. S. Davidson and B. Milwidsky, Synthetic Detergents , Seventh Edition, John Wiley and Sons, New York, 1987.
  • compositions of this invention may also contain formulation auxiliaries and additives, known to those skilled in the art as formulation aids (some of which may be considered to also function as solid diluents, liquid diluents or surfactants).
  • formulation auxiliaries and additives may control: pH (buffers), foaming during processing (antifoams such polyorganosiloxanes), sedimentation of active ingredients (suspending agents), viscosity (thixotropic thickeners), in-container microbial growth (antimicrobials), product freezing (antifreezes), color (dyes/pigment dispersions), wash-off (film formers or stickers), evaporation (evaporation retardants), and other formulation attributes.
  • Film formers include, for example, polyvinyl acetates, polyvinyl acetate copolymers, polyvinylpyrrolidone-vinyl acetate copolymer, polyvinyl alcohols, polyvinyl alcohol copolymers and waxes.
  • formulation auxiliaries and additives include those listed in McCutcheon's Volume 2 : Functional Materials , annual International and North American editions published by McCutcheon's Division, The Manufacturing Confectioner Publishing Co.; and PCT Publication WO 03/024222.
  • the compounds of Formula 1 and other active ingredients are typically incorporated into the present compositions by dissolving the active ingredient in a solvent or by grinding in a liquid or dry diluent.
  • Solutions, including emulsifiable concentrates can be prepared by simply mixing the ingredients. If the solvent of a liquid composition intended for use as an emulsifiable concentrate is water-immiscible, an emulsifier is typically added to emulsify the active-containing solvent upon dilution with water.
  • Active ingredient slurries, with particle diameters of up to 2,000 ⁇ m can be wet milled using media mills to obtain particles with average diameters below 3 ⁇ m.
  • Aqueous slurries can be made into finished suspension concentrates (see, for example, U.S. Pat. No. 3,060,084) or further processed by spray drying to form water-dispersible granules. Dry formulations usually require dry milling processes, which produce average particle diameters in the 2 to 10 ⁇ m range. Dusts and powders can be prepared by blending and usually grinding (such as with a hammer mill or fluid-energy mill). Granules and pellets can be prepared by spraying the active material upon preformed granular carriers or by agglomeration techniques. See Browning, “Agglomeration”, Chemical Engineering , Dec.
  • Pellets can be prepared as described in U.S. Pat. No. 4,172,714.
  • Water-dispersible and water-soluble granules can be prepared as taught in U.S. Pat. No. 4,144,050, U.S. Pat. No. 3,920,442 and DE 3,246,493.
  • Tablets can be prepared as taught in U.S. Pat. No. 5,180,587, U.S. Pat. No. 5,232,701 and U.S. Pat. No. 5,208,030.
  • Films can be prepared as taught in GB 2,095,558 and U.S. Pat. No. 3,299,566.
  • Component (b1a) refers to 1-[4-[4-[5-(2,6-difluorophenyl)-4,5-dihydro-3-isoxazolyl]-2-thiazolyl]-1-piperidinyl]-2-[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]ethanone.
  • Wettable Powder Any one of Compounds 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 and 12 59.1% Component (b3a) 5.9% dodecylphenol polyethylene glycol ether 2.0% sodium ligninsulfonate 4.0% sodium silicoaluminate 6.0% montmorillonite (calcined) 23.0%
  • Granule Any one of Compounds 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 and 12 5.0% Component (b4a) 5.0% attapulgite granules (low volatile matter, 90.0% 0.71/0.30 mm; U.S.S. No. 25-50 sieves)
  • Emulsifiable Concentrate Any one of Compounds 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 and 12 6.7% Component (b6a) 3.3% polyoxyethylene sorbitol hexoleate 20.0% C 6 -C 10 fatty acid methyl ester 70.0%
  • Component (b7) 2.5% polyvinylpyrrolidone-vinyl acetate copolymer 30.0% alkylpolyglycoside 30.0% glyceryl monooleate 15.0% water 20.0%
  • Granule Any one of Compounds 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 and 12 5.0% Component (b9a) 5.0% attapulgite granules (low volatile matter, 90.0% 0.71/0.30 mm; U.S.S. No. 25-50 sieves)
  • Emulsifiable Concentrate Any one of Compounds 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 and 12 5.0% Component (b11) 5.0% polyoxyethylene sorbitol hexoleate 20.0% C 6 -C 10 fatty acid methyl ester 70.0%
  • Component (b12) 18.95% polyvinylpyrrolidone-vinyl acetate copolymer 5.00% montan acid wax 5.00% calcium ligninsulfonate 1.00% polyoxyethylene/polyoxypropylene block copolymers 1.00% stearyl alcohol (POE 20) 2.00% polyorganosilane 0.20% colorant red dye 0.05% water 65.75%
  • Emulsifiable Concentrate Any one of Compounds 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 and 12 5.0% Component (b13) 5.0% polyoxyethylene sorbitol hexoleate 20.0% C 6 -C 10 fatty acid methyl ester 70.0%
  • combinations of components (a), (b) and optionally (c) can be together or separately formulated with at least one of a surfactant, a solid diluent or a liquid diluent.
  • a surfactant e.g., sodium bicarbonate
  • a solid diluent e.g., sodium bicarbonate
  • a liquid diluent e.g., sodium bicarbonate
  • two or all three of components (a), (b) and (c) can be formulated together to form a premix composition, or they can be formulated separately and then the formulated compositions combined together before application (e.g., in a spray tank) or, alternatively, applied in succession.
  • compositions containing components (a), (b) or (c) are present in biologically effective amounts, or more particularly, for example, fungicidally effective amounts if they are fungicidal or insecticidally effective amounts if they are insecticidal.
  • Formulations are often diluted with water to form aqueous compositions before application.
  • Aqueous compositions for direct applications to the plant or portion thereof typically comprise at least about 1 ppm or more (e.g., from 1 ppm to 100 ppm) of fungicidally active compounds according to the present invention.
  • compositions of this invention are useful as plant disease control agents.
  • the present invention therefore further comprises a method for controlling plant diseases caused by fungal plant pathogens comprising applying to the plant or portion thereof to be protected, or to the plant seed or vegetative propagation unit to be protected, an effective amount of a composition of the invention (e.g., a composition comprising component (a), or components (a) and (b), or components (a), (b) and (c)).
  • This aspect of the present invention can also be described as a method for protecting a plant or plant seed from diseases caused by fungal pathogens comprising applying a fungicidally effective amount of a composition of the invention to the plant (or portion thereof) or plant seed (directly or through the environment (e.g., growing medium) of the plant or plant seed).
  • Component (a) compounds and/or combinations thereof with component (b) compounds and/or (c) one or more other biologically active compounds or agents can be applied to plants genetically transformed to express proteins toxic to invertebrate pests (such as Bacillus thuringiensis delta-endotoxins).
  • proteins toxic to invertebrate pests such as Bacillus thuringiensis delta-endotoxins.
  • the effect of the exogenously applied present component (a) alone or in combination with component (b) and optionally component (c) may be synergistic with the expressed toxin proteins.
  • Plant disease control is ordinarily accomplished by applying an effective amount of a composition of the invention (e.g., comprising component (a), or a mixture of components (a), (b) and optionally (c)), typically as a formulated composition, either pre- or post-infection, to the portion of the plant to be protected such as the roots, stems, foliage, fruit, seeds, tubers or bulbs, or to the media (soil or sand) in which the plants to be protected are growing.
  • Component (a) or mixtures thereof can also be applied to seeds to protect the seeds and seedlings developing from the seeds. The mixtures can also be applied through irrigation water to treat plants.
  • Control of postharvest pathogens which infect the produce before harvest is typically accomplished by field application of a composition of the invention, and in cases where infection occurs after harvest the compositions can be applied to the harvested crop as dips, sprays, fumigants, treated wraps or box liners.
  • Suitable rates of application e.g., fungicidally effective amounts
  • component (a) i.e. at least one compound selected from compounds of Formula 1, N-oxides and salts thereof
  • suitable rates of application e.g., biologically effective amounts, fungicidally effective amounts or insecticidally effective amounts
  • Foliage can normally be protected when treated at a rate of from less than about 1 g/ha to about 5,000 g/ha of active ingredients.
  • Seed and seedlings can normally be protected when seed is treated at a rate of from about 0.1 to about 10 g per kilogram of seed; and vegetative propagation units (e.g., cuttings and tubers) can normally be protected when propagation unit is treated at a rate of from about 0.1 to about 10 g per kilogram of propagation unit.
  • vegetative propagation units e.g., cuttings and tubers
  • propagation unit is treated at a rate of from about 0.1 to about 10 g per kilogram of propagation unit.
  • One skilled in the art can easily determine through simple experimentation the application rates of component (a), and mixtures and compositions thereof, containing particular combinations of active ingredients according to this invention needed to provide the desired spectrum of plant protection and control of plant diseases and optionally other plant pests.
  • the compounds of Formula 1, N-oxides, and salts thereof, are particularly efficacious for controlling plant diseases caused by fungal pathogens, particularly in the Basidomycete and Ascomycete classes. Combining these compounds with other fungicidal compounds can provide control of diseases caused by a broad spectrum of fungal plant pathogens in the Basidiomycete, Ascomycete, Oomycete and Deuteromycete classes.
  • mixtures and compositions described herein can control a broad spectrum of plant diseases, foliar pathogens of crops including: cereal grain crops such as wheat, barley, oats, rye, triticale, rice, maize, sorghum and millet; vine crops such as table and wine grapes; field crops such as oilseed rape (canola), sunflower; sugar beets, sugar cane, soybean, peanuts (groundnut), tobacco, alfalfa, clover, lespedeza, trefoil and vetch; pome fruits such as apple, pear, crabapple, loquat, mayhaw and quince; stone fruits such as peaches, cherries, plums, apricots, nectarines and almonds; citrus fruits such as lemons, limes, oranges, grapefruit, mandarin (tangerines) and kumquat; root and tuber vegetables and field crops (and their foliage) such as artichoke, garden and sugar beet, carrot, cassava, ginger,
  • pathogens include: Oomycetes, including Phytophthora pathogens such as Phytophthora infestans, Phytophthora megasperma, Phytophthora parasitica, Phytophthora cinnamomi and Phytophthora capsici, Pythium pathogens such as Pythium aphanidermatum , and pathogens in the Peronosporaceae family such as Plasmopara viticola, Peronospora spp. (including Peronospora tabacina and Peronospora parasitica ), Pseudoperonospora spp.
  • Phytophthora pathogens such as Phytophthora infestans, Phytophthora megasperma, Phytophthora parasitica, Phytophthora cinnamomi and Phytophthora capsici
  • Pythium pathogens such as Pythium aphanidermatum
  • Botrytis pathogens such as Botrytis cinerea, Monilinia fructicola, Sclerotinia pathogens such as Sclerotinia sclerotiorum and Sclerotinia minor, Magnaporthe grisea, Phomopsis viticola, Helminthosporium pathogens such as Helminthosporium tritici repentis, Pyrenophora teres , anthracnose disease pathogens such as Glomerella or Colletotrichum spp.
  • Botrytis pathogens such as Botrytis cinerea, Monilinia fructicola, Sclerotinia pathogens such as Sclerotinia sclerotiorum and Sclerotinia minor, Magnaporthe grisea, Phomopsis viticola, Helminthosporium pathogens such as Helminthosporium tritici repentis, Pyrenophora teres , anthracnose disease pathogens such as Glo
  • Rhizoctonia spp such as Colletotrichum graminicola and Colletotrichum orbiculare ), and Gaeumannomyces graminis ; Basidiomycetes, including rust diseases caused by Puccinia spp. (such as Puccinia recondita, Puccinia striiformis, Puccinia hordei, Puccinia graminis and Puccinia arachidis ), Hemileia vastatrix and Phakopsora pachyrhizi ; other pathogens including Rhizoctonia spp.
  • Puccinia recondita Puccinia striiformis, Puccinia hordei, Puccinia graminis and Puccinia arachidis
  • Hemileia vastatrix and Phakopsora pachyrhizi other pathogens including Rhizoctonia spp.
  • Rhizoctonia solani and Rhizoctonia oryzae Fusarium pathogens such as Fusarium roseum, Fusarium graminearum and Fusarium oxysporum; Verticillium dahliae; Sclerotium rolfsii; Rynchosporium secalis; Cercosporidium personatum, Cercospora arachidicola and Cercospora beticola; Rutstroemia floccosum (also known as Sclerontina homoeocarpa ); Rhizopus spp. (such as Rhizopus stolonifer ); Aspergillus spp.
  • pathogens are referred to as diseases, and thus in the preceding sentence the word “pathogen” also refers to the plant disease caused by the pathogen. More precisely, plant diseases are caused by pathogens. Therefore, for example, powdery mildew diseases are plant diseases caused by powdery mildew pathogens, Septoria diseases are plant diseases caused by Septoria pathogens, and rust diseases are plant diseases caused by rust disease pathogens.
  • Certain fungicidal compounds are also bactericidal, and therefore in addition to their fungicidal activity, the compositions or combinations can also have activity against bacteria such as Erwinia amylovora, Xanthomonas campestris, Pseudomonas syringae , and other related species.
  • compounds of Formula 1 and their mixtures and compositions according to this invention are useful in treating postharvest diseases of fruits and vegetables caused by fungi and bacteria. These infections can occur before, during and after harvest. For example, infections can occur before harvest and then remain dormant until some point during ripening (e.g., host begins tissue changes in such a way that infection can progress); also infections can arise from surface wounds created by mechanical or insect injury.
  • treatment of postharvest diseases with compounds of the invention can increase the period of time during which perishable edible plant parts (e.g., fruits, seeds, foliage, stems, bulbs, tubers) can be stored refrigerated or unrefrigerated after harvest, and remain edible and free from noticeable or harmful degradation or contamination by fungi or other microorganisms.
  • perishable edible plant parts e.g., fruits, seeds, foliage, stems, bulbs, tubers
  • Treatment of edible plant parts before or after harvest with compounds, mixtures or compositions according to this invention can also decrease the formation of toxic metabolites of fungi or other microorganisms, for example, mycotoxins such as aflatoxins.
  • compositions are provided in accordance with this invention that comprise proportions of component (a) and component (b) that are especially useful for controlling particular fungal diseases (such as Alternaria solani, Blumeria graminis f. sp. tritici, Botrytis cinerea, Puccinia recondita f. sp. tritici, Rhizoctonia solani, Septoria nodorum, Septoria tritici ).
  • particular fungal diseases such as Alternaria solani, Blumeria graminis f. sp. tritici, Botrytis cinerea, Puccinia recondita f. sp. tritici, Rhizoctonia solani, Septoria nodorum, Septoria tritici ).
  • Mixtures of fungicides may also provide significantly better disease control than could be predicted based on the activity of the individual components.
  • This synergism has been described as “the cooperative action of two components of a mixture, such that the total effect is greater or more prolonged than the sum of the effects of the two (or more) taken independently” (see P. M. L. Tames, Neth. J. Plant Pathology 1964, 70, 73-80).
  • active ingredients e.g., fungicidal compounds
  • the active ingredients are applied in a synergistic weight ratio and synergistic (i.e. synergistically effective) amounts.
  • Tests include tests demonstrating the efficacy of compounds of Fomrula 1 for controlling specific pathogens; this efficacy is thus provided to fungicidal mixtures comprising these compounds.
  • the disease control afforded by the present compounds alone or in mixtures is not limited, however, to the pathogenic fungi species exemplified.
  • Mass spectra are reported as the molecular weight of the highest isotopic abundance parent ion (M+1) formed by addition of H + (molecular weight of 1) to the molecule, observed by mass spectrometry using atmospheric pressure chemical ionization (AP + ). The presence of molecular ions containing one or more higher atomic weight isotopes of lower abundance (e.g., 37 Cl, 81 Br) is not reported.
  • test suspensions for Tests A-I were first dissolved in acetone in an amount equal to 3% of the final volume and then suspended at the desired concentration (in ppm) in acetone and purified water (50/50 mix by volume) containing 250 ppm of the surfactant Trem® 014 (polyhydric alcohol esters). The resulting test suspensions were then used in Tests A-I. Each test was conducted in triplicate, and the results were averaged. Spraying a 200 ppm test suspension to the point of run-off on the test plants was the equivalent of a rate of about 800 g/ha. Unless otherwise indicated, the rating values indicate a 200 ppm test suspension was used. (An asterisk “*” next to the rating value indicates a 40 ppm test suspension was used.)
  • test suspension was sprayed to the point of run-off on tomato seedlings.
  • seedlings were inoculated with a spore suspension of Botrytis cinerea (the causal agent of tomato Botrytis ) and incubated in saturated atmosphere at 20° C. for 48 h, and then moved to a growth chamber at 24° C. for 3 additional days, after which time visual disease ratings were made.
  • Botrytis cinerea the causal agent of tomato Botrytis
  • test suspension was sprayed to the point of run-off on tomato seedlings.
  • seedlings were inoculated with a spore suspension of Alternaria solani (the causal agent of tomato early blight) and incubated in a saturated atmosphere at 27° C. for 48 h, and then moved to a growth chamber at 20° C. for 5 days, after which time visual disease ratings were made.
  • Alternaria solani the causal agent of tomato early blight
  • test suspension was sprayed to the point of run-off on tomato seedlings.
  • seedlings were inoculated with a spore suspension of Phytophthora infestans (the causal agent of tomato late blight) and incubated in a saturated atmosphere at 20° C. for 24 h, and then moved to a growth chamber at 20° C. for 5 days, after which time visual disease ratings were made.
  • Phytophthora infestans the causal agent of tomato late blight
  • test suspension was sprayed to the point of run-off on creeping bent grass ( Agrostis sp.) seedlings.
  • test suspension was sprayed to the point of run-off on wheat seedlings.
  • seedlings were inoculated with a spore suspension of Septoria nodorum (the causal agent of Septoria glume blotch) and incubated in a saturated atmosphere at 24° C. for 48 h, and then moved to a growth chamber at 20° C. for 9 days, after which time visual disease ratings were made.
  • Septoria nodorum the causal agent of Septoria glume blotch
  • test suspension was sprayed to the point of run-off on wheat seedlings.
  • seedlings were inoculated with a spore suspension of Septoria tritici (the causal agent of wheat leaf blotch) and incubated in saturated atmosphere at 24° C. for 48 h. and then the seedlings were moved to a growth chamber at 20° C. for 19 additional days, after which time visual disease ratings were made.
  • Wheat seedlings were inoculated with a spore suspension of Puccinia recondita f. sp. tritici (the causal agent of wheat leaf rust) and incubated in a saturated atmosphere at 20° C. for 24 h, and then moved to a growth chamber at 20° C. for 2 days. At the end of this time the test suspension was sprayed to the point of run-off, and then the seedlings were moved to a growth chamber at 20° C. for 4 days after which time visual disease ratings were made.
  • Puccinia recondita f. sp. tritici the causal agent of wheat leaf rust
  • test suspension was sprayed to the point of run-off on wheat seedlings.
  • seedlings were inoculated with a spore suspension of Puccinia recondita f. sp. tritici (the causal agent of wheat leaf rust) and incubated in a saturated atmosphere at 20° C. for 24 h, and then moved to a growth chamber at 20° C. for 6 days, after which time visual disease ratings were made.
  • test suspension was sprayed to the point of run-off on wheat seedlings.
  • seedlings were inoculated with a spore dust of Blumeria graminis f. sp. tritici (also known as Erysiphe graminis f. sp. tritici , the causal agent of wheat powdery mildew) and incubated in a growth chamber at 20° C. for 8 days, after which time visual disease ratings were made.
  • Blumeria graminis f. sp. tritici also known as Erysiphe graminis f. sp. tritici , the causal agent of wheat powdery mildew
  • Results for Tests A-I are given in Table A.
  • a rating of 100 indicates 100% disease control and a rating of 0 indicates no disease control (relative to the controls).
  • a hyphen (-) indicates no test results.
  • test results presented in Table A for compounds of Formula 1 illustrate the fungicidal activity of component (a) contributing to the plant disease control utility of compositions comprising component (a) in combination with component (b) and optionally component (c) according to the present invention.

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Abstract

Disclosed is a fungicidal composition comprising (a) at least one compound selected from the compounds of Formula 1, N-oxides, and salts thereof,
Figure US20150018374A1-20150115-C00001
wherein
    • R1 is F, Cl or Br;
    • R2 is H or F; and
    • R3 is Cl or Br; and
      (b) at least one fungicidal compound selected from (b1) through (b13) as disclosed herein. Also disclosed is a method for controlling plant diseases caused by fungal plant pathogens comprising applying to the plant or portion thereof, or to the plant seed, a fungicidally effective amount of a compound of Formula 1, an N-oxide, or salt thereof (e.g., as a component in the aforesaid composition). Also disclosed are process intermediate compounds useful for preparing compounds of Formula 1.

Description

    FIELD OF THE INVENTION
  • This invention relates to certain pyrazole derivatives, their N-oxides and salts, to process intermediates for their preparation and to mixtures and compositions comprising such pyrazole derivatives and methods for using such pyrazole derivatives and their mixtures and compositions as fungicides.
    • BACKGROUND OF THE INVENTION
  • The control of plant diseases caused by fungal plant pathogens is extremely important in achieving high crop efficiency. Plant disease damage to ornamental, vegetable, field, cereal and fruit crops can cause significant reduction in productivity and thereby result in increased costs to the consumer. In addition to often being highly destructive, plant diseases can be difficult to control and may develop resistance to commercial fungicides. Many products are commercially available for these purposes, but the need continues for new fungicidal compounds which are more effective, less costly, less toxic, environmentally safer or have different sites of action. Besides introduction of new fungicides, combinations of fungicides are often used to facilitate disease control, to broaden spectrum of control and to retard resistance development. Furthermore, certain rare combinations of fungicides demonstrate a greater-than-additive (i.e. synergistic) effect to provide commercially important levels of plant disease control. The advantages of particular fungicide combinations are recognized in the art to vary, depending on such factors as the particular plant species and plant disease to be treated, and whether the plants are treated before or after infection with the fungal plant pathogen. Accordingly new advantageous combinations are needed to provide a variety of options to best satisfy particular plant disease control needs. Such combinations have now been discovered. U.S. Patent Publication US 2011/0319430 A1 discloses certain fungicidal pyrazoles, but does not disclose the fungicidal mixtures of the present invention.
    • SUMMARY OF THE INVENTION
  • This invention relates to a fungicidal composition (i.e. combination, mixture) comprising
  • (a) at least one compound selected from the compounds of Formula 1 (including all stereoisomers), N-oxides, and salts thereof:
  • Figure US20150018374A1-20150115-C00002
  • wherein
      • R1 is F, Cl or Br;
      • R2 is H or F; and
      • R3 is Cl or Br; and
        (b) at least one fungicidal compound selected from
  • Figure US20150018374A1-20150115-C00003
      • wherein Rb20 and Rb21 are independently CH3, CF2H or CF3; each Rb22 is independently halogen or cyano; n is 0, 1, 2 or 3; and L is a direct bond or —CH2O— wherein the left bond is connected to the dihydroisoxazole ring and the right bond is connected to the phenyl ring (in Formula B1);
  • Figure US20150018374A1-20150115-C00004
        • wherein Rb1 is
  • Figure US20150018374A1-20150115-C00005
      • wherein Rb2 is —CH2OC(O)CH(CH3)2, —C(O)CH3, —CH2OC(O)CH3, —C(O)OCH2CH(CH3)2 or
  • Figure US20150018374A1-20150115-C00006
      • wherein Rb3 is CH3 or F;
  • Figure US20150018374A1-20150115-C00007
      • wherein Rb4 is —(CH2)4CH3, —C(CH3)3 or —(CH2)2C≡CH;
  • Figure US20150018374A1-20150115-C00008
      • wherein Rb5 is H or F, and Rb6 is —CF2CHFCF3 or —CF2CF2H;
  • Figure US20150018374A1-20150115-C00009
      • wherein
      • Rb7 is
  • Figure US20150018374A1-20150115-C00010
      • Rb8 is H, halogen or C1-C2 alkyl;
      • Rb9 is C1-C8 alkyl, C1-C8 haloalkyl or C2-C8 alkoxyalkyl;
      • Rb10 is halogen, C1-C2 alkyl or C1-C2 haloalkyl;
      • Rb11 is halogen, C1-C2 alkyl or C1-C2 haloalkyl;
      • Rb12 is C1-C2 alkyl;
      • Rb13 is H, halogen or C1-C2 alkyl;
      • Rb14 is C1-C2 alkyl or C1-C2 haloalkyl;
      • Rb15 is H, C1-C2 alkyl or C1-C2 haloalkyl;
      • W is CH or N;
      • Y is CH or N; and
      • Z is CH or N;
  • Figure US20150018374A1-20150115-C00011
  • and salts thereof.
  • This invention also relates to a fungicidal composition comprising: (a) at least one compound selected from the compounds of Formula 1, (b) at least one fungicidal compound selected from Formulae B1 through B13 and salts thereof described above, and further comprising (c) at least one additional compound or agent that is biologically active.
  • This invention also relates to a composition comprising one of the aforesaid compositions comprising components (a) and (b) and at least one additional component selected from the group consisting of surfactants, solid diluents and liquid diluents.
  • This invention also relates to a method for controlling plant diseases caused by fungal plant pathogens comprising applying to the plant or portion thereof, or to the plant seed, a fungicidally effective amount of one of the aforesaid compositions.
  • The aforedescribed method can also be described as a method for protecting a plant or plant seed from diseases caused by fungal pathogens comprising applying a fungicidally effective amount of one of the aforesaid compositions to the plant (or portion thereof) or plant seed (directly or through the environment (e.g., growing medium) of the plant or plant seed).
  • This invention also relates to a compound of Formula 1 described above, or an N-oxide or salt thereof. This invention further relates to a fungicidal composition comprising a compound of Formula 1, or an N-oxide or salt thereof, and at least one additional component selected from the group consisting of surfactants, solid diluents and liquid diluents. This invention also further relates to a method for protecting a plant or plant seed from diseases caused by fungal pathogens comprising a fungicidally effective amount of a compound of Formula 1, or an N-oxide or salt thereof, to the plant or plant seed.
  • This invention further relates to a compound of Formula 14,
  • Figure US20150018374A1-20150115-C00012
  • wherein R3 is Cl or Br.
  • This invention further relates to a compound of Formula 17,
  • Figure US20150018374A1-20150115-C00013
  • wherein
      • R1 is F, Cl or Br;
      • R2 is H or F;
      • R3 is Cl or Br; and
      • R32 is H, CH3, CH2CH3 or (CH2)2CH3; particularly
        provided that when R1 is H, or when R1 and R2 are each F, then R32 is H.
  • This invention further relates to a compound of Formula 20,
  • Figure US20150018374A1-20150115-C00014
  • wherein R1 is F, Cl or Br, and R2 is H or F, particularly wherein R1 is Br and R2 is F.
  • This invention further relates to a compound of Formula 22,
  • Figure US20150018374A1-20150115-C00015
  • wherein R1 is F, Cl or Br; R2 is H or F; R3 is Cl or Br; and M is Na or K.
    Compounds of Formulae 14, 17, 20 and 22 can be used as process intermediates to prepare compounds of Formula 1, which are useful as component (a) in the present compositions.
    • DETAILS OF THE INVENTION
  • As used herein, the terms “comprises,” “comprising,” “includes,” “including,” “has,” “having,” “contains”, “containing,” “characterized by” or any other variation thereof, are intended to cover a non-exclusive inclusion, subject to any limitation explicitly indicated. For example, a composition, mixture, process or method that comprises a list of elements is not necessarily limited to only those elements but may include other elements not expressly listed or inherent to such composition, mixture, process or method.
  • The transitional phrase “consisting of” excludes any element, step, or ingredient not specified. If in the claim, such would close the claim to the inclusion of materials other than those recited except for impurities ordinarily associated therewith. When the phrase “consisting of” appears in a clause of the body of a claim, rather than immediately following the preamble, it limits only the element set forth in that clause; other elements are not excluded from the claim as a whole.
  • The transitional phrase “consisting essentially of” is used to define a composition or method that includes materials, steps, features, components, or elements, in addition to those literally disclosed, provided that these additional materials, steps, features, components, or elements do not materially affect the basic and novel characteristic(s) of the claimed invention. The term “consisting essentially of” occupies a middle ground between “comprising” and “consisting of”.
  • Where applicants have defined an invention or a portion thereof with an open-ended term such as “comprising,” it should be readily understood that (unless otherwise stated) the description should be interpreted to also describe such an invention using the terms “consisting essentially of” or “consisting of”.
  • Further, unless expressly stated to the contrary, “or” refers to an inclusive or and not to an exclusive or. For example, a condition A or B is satisfied by any one of the following: A is true (or present) and B is false (or not present), A is false (or not present) and B is true (or present), and both A and B are true (or present).
  • Also, the indefinite articles “a” and “an” preceding an element or component of the invention are intended to be nonrestrictive regarding the number of instances (i.e. occurrences) of the element or component. Therefore “a” or “an” should be read to include one or at least one, and the singular word form of the element or component also includes the plural unless the number is obviously meant to be singular.
  • As referred to in the present disclosure and claims, “plant” includes members of Kingdom Plantae, particularly seed plants (Spermatopsida), at all life stages, including young plants (e.g., germinating seeds developing into seedlings) and mature, reproductive stages (e.g., plants producing flowers and seeds). Portions of plants include geotropic members typically growing beneath the surface of the growing medium (e.g., soil), such as roots, tubers, bulbs and corms, and also members growing above the growing medium, such as foliage (including stems and leaves), flowers, fruits and seeds.
  • As referred to herein, the term “seedling”, used either alone or in a combination of words means a young plant developing from the embryo of a seed.
  • The term “Registry Number” refers to Chemical Abstracts Registry Number.
  • A single bond drawn as a wavy line (e.g., in Formulae 17 and 22) denote that either the E or Z isomer or a mixture of E and Z isomers may be present. A dashed line perpendicularly traversing a bond denotes that the bond connects the substituent fragment to the remainder of a molecule (e.g., Rb1 in Formula B2).
  • Compounds relevant to the compositions and methods of this invention can exist as one or more stereoisomers. The various stereoisomers include enantiomers, diastereomers, atropisomers and geometric isomers. One skilled in the art will appreciate that one stereoisomer may be more active and/or may exhibit beneficial effects when enriched relative to the other stereoisomer(s) or when separated from the other stereoisomer(s). Additionally, the skilled artisan knows how to separate, enrich, and/or to selectively prepare said stereoisomers. The compounds in the compositions of this invention may be present as a mixture of stereoisomers, individual stereoisomers or as an optically active form.
  • Synthetic methods for the preparation of N-oxides of heterocycles such as pyrazoles are very well known by one skilled in the art including the oxidation of heterocycles with peroxy acids such as peracetic and m-chloroperbenzoic acid (MCPBA), hydrogen peroxide, alkyl hydroperoxides such as t-butyl hydroperoxide, sodium perborate, and dioxiranes such as dimethyldioxirane. These methods for the preparation of N-oxides have been extensively described and reviewed in the literature, see for example: T. L. Gilchrist in Comprehensive Organic Synthesis, vol. 7, pp 748-750, S. V. Ley, Ed., Pergamon Press; M. Tisler and B. Stanovnik in Comprehensive Heterocyclic Chemistry, vol. 3, pp 18-20, A. J. Boulton and A. McKillop, Eds., Pergamon Press; M. R. Grimmett and B. R. T. Keene in Advances in Heterocyclic Chemistry, vol. 43, pp 149-161, A. R. Katritzky, Ed., Academic Press; M. Tisler and B. Stanovnik in Advances in Heterocyclic Chemistry, vol. 9, pp 285-291, A. R. Katritzky and A. J. Boulton, Eds., Academic Press; and G. W. H. Cheeseman and E. S. G. Werstiuk in Advances in Heterocyclic Chemistry, vol. 22, pp 390-392, A. R. Katritzky and A. J. Boulton, Eds., Academic Press.
  • One skilled in the art recognizes that because in the environment and under physiological conditions salts of chemical compounds are in equilibrium with their corresponding nonsalt forms, salts share the biological utility of the nonsalt forms. Thus a wide variety of salts of the compounds of Formula 1 alone and in mixtures are useful for control of plant diseases caused by fungal plant pathogens (i.e. are agriculturally suitable). The salts of the compounds of Formula 1 include acid-addition salts with inorganic or organic acids such as hydrobromic, hydrochloric, nitric, phosphoric, sulfuric, acetic, butyric, fumaric, lactic, maleic, malonic, oxalic, propionic, salicylic, tartaric, 4-toluenesulfonic or valeric acids. Accordingly, the present invention relates to mixtures of compounds selected from Formula 1, N-oxides and agriculturally suitable salts thereof. Also, biologically similar salt forms can exist for many of the compounds of Formulae B1 through B13.
  • Compounds selected from Formula 1, stereoisomers, tautomers, N-oxides, and salts thereof, typically exist in more than one form, and Formula 1 thus includes all crystalline and non-crystalline forms of the compounds that Formula 1 represents. Non-crystalline forms include embodiments which are solids such as waxes and gums as well as embodiments which are liquids such as solutions and melts. Crystalline forms include embodiments which represent essentially a single crystal type and embodiments which represent a mixture of polymorphs (i.e. different crystalline types). The term “polymorph” refers to a particular crystalline form of a chemical compound that can crystallize in different crystalline forms, these forms having different arrangements and/or conformations of the molecules in the crystal lattice. Although polymorphs can have the same chemical composition, they can also differ in composition due the presence or absence of co-crystallized water or other molecules, which can be weakly or strongly bound in the lattice. Polymorphs can differ in such chemical, physical and biological properties as crystal shape, density, hardness, color, chemical stability, melting point, hygroscopicity, suspensibility, dissolution rate and biological availability. One skilled in the art will appreciate that a polymorph of a compound represented by Formula 1 can exhibit beneficial effects (e.g., suitability for preparation of useful formulations, improved biological performance) relative to another polymorph or a mixture of polymorphs of the same compound represented by Formula 1. Preparation and isolation of a particular polymorph of a compound represented by Formula 1 can be achieved by methods known to those skilled in the art including, for example, crystallization using selected solvents and temperatures. Compounds of Formulae B1 through B13, including salts thereof, can also typically exist in more than one form.
  • In the embodiments of the present invention, including those described below, reference to Formula 1 includes N-oxides and salts thereof unless otherwise indicated, and reference to “a compound of Formula 1” includes the definitions of substituents specified in the Summary of the Invention unless further defined in the Embodiments. Furthermore, reference to Formulae B1 through B13 includes salts thereof unless otherwise indicated.
    • Embodiment 1
  • A composition comprising components (a) and (b) described in the Summary of the Invention wherein in Formula 1, R2 is F.
    • Embodiment 2
  • A composition comprising components (a) and (b) described in the Summary of the Invention wherein in Formula 1, R2 is H.
    • Embodiment 3
  • A composition comprising components (a) and (b) described in the Summary of the Invention or Embodiment 1 or 2 wherein component (a) does not comprise an N-oxide of a compound of Formula 1.
    • Embodiment 4
  • A composition comprising components (a) and (b) described in the Summary of the Invention or Embodiment 3 wherein component (a) comprises a compound selected from the group consisting of
    • 4-(2-chloro-4-fluorophenyl)-N-(2-fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine (Compound 1),
    • 4-(2-chloro-4-fluorophenyl)-N-(2-chlorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine (Compound 10),
    • N-(2-bromophenyl)-4-(2-chloro-4-fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine (Compound 9),
    • 4-(2-bromo-4-fluorophenyl)-N-(2-fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine (Compound 12),
    • 4-(2-bromo-4-fluorophenyl)-N-(2-chlorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine (Compound 8),
    • 4-(2-bromo-4-fluorophenyl)-N-(2-bromophenyl)-1,3-dimethyl-1H-pyrazol-5-amine (Compound 6),
    • 4-(2-chloro-4-fluorophenyl)-N-(2,6-difluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine (Compound 2),
    • 4-(2-chloro-4-fluorophenyl)-N-(2-chloro-6-fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine (Compound 3),
    • N-(2-bromo-6-fluorophenyl)-4-(2-chloro-4-fluoromethyl)-1,3-dimethyl-1H-pyrazol-5-amine (Compound 5),
    • 4-(2-bromo-4-fluorophenyl)-N-(2,6-difluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine (Compound 11),
    • 4-(2-bromo-4-fluorophenyl)-N-(2-chloro-6-fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine (Compound 4), and
    • 4-(2-bromo-4-fluorophenyl)-N-(2-bromo-6-fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine (Compound 7)
  • (wherein the compound numbers are identified in Index Table A).
    • Embodiment 5
  • A composition of Embodiment 4 wherein component (a) comprises Compound 1.
    • Embodiment 6
  • A composition of Embodiment 4 wherein component (a) comprises Compound 2.
    • Embodiment 7
  • A composition of Embodiment 4 wherein component (a) comprises Compound 3.
    • Embodiment 8
  • A composition of Embodiment 4 wherein component (a) comprises Compound 4.
    • Embodiment 9
  • A composition of Embodiment 4 wherein component (a) comprises Compound 5.
    • Embodiment 10
  • A composition of Embodiment 4 wherein component (a) comprises Compound 6.
    • Embodiment 11
  • A composition of Embodiment 4 wherein component (a) comprises Compound 7.
    • Embodiment 12
  • A composition of Embodiment 4 wherein component (a) comprises Compound 8.
    • Embodiment 13
  • A composition of Embodiment 4 wherein component (a) comprises Compound 9.
    • Embodiment 14
  • A composition of Embodiment 4 wherein component (a) comprises Compound 10.
    • Embodiment 15
  • A composition of Embodiment 4 wherein component (a) comprises Compound 11.
    • Embodiment 16
  • A composition of Embodiment 4 wherein component (a) comprises Compound 12.
    • Embodiment 17
  • A composition comprising components (a) and (b) described in the Summary of the Invention or any one of Embodiments 1 through 16 wherein component (b) comprises at least one fungicidal compound selected from (b1).
    • Embodiment 17a
  • A composition comprising components (a) and (b) described in the Summary of the Invention or any one of Embodiments 1 through 17 wherein component (b) comprises at least one fungicidal compound selected from (b1a).
    • Embodiment 17b
  • A composition comprising components (a) and (b) described in the Summary of the Invention or any one of Embodiments 1 through 17a wherein component (b) comprises at least one fungicidal compound selected from (b1b).
    • Embodiment 18
  • A composition comprising components (a) and (b) described in the Summary of the Invention or any one of Embodiments 1 through 17b wherein component (b) comprises at least one fungicidal compound selected from (b2).
    • Embodiment 19
  • A composition comprising components (a) and (b) described in the Summary of the Invention or any one of Embodiments 1 through 18 wherein component (b) comprises at least one fungicidal compound selected from (b3).
    • Embodiment 20
  • A composition comprising components (a) and (b) described in the Summary of the Invention or any one of Embodiments 1 through 19 wherein component (b) comprises at least one fungicidal compound selected from (b4).
    • Embodiment 21
  • A composition comprising components (a) and (b) described in the Summary of the Invention or any one of Embodiments 1 through 20 wherein component (b) comprises at least one fungicidal compound selected from (b5).
    • Embodiment 22
  • A composition comprising components (a) and (b) described in the Summary of the Invention or any one of Embodiments 1 through 21 wherein component (b) comprises at least one fungicidal compound selected from (b6).
    • Embodiment 23
  • A composition comprising components (a) and (b) described in the Summary of the Invention or any one of Embodiments 1 through 22 wherein component (b) comprises at least one fungicidal compound selected from (b7).
    • Embodiment 24
  • A composition comprising components (a) and (b) described in the Summary of the Invention or any one of Embodiments 1 through 23 wherein component (b) comprises at least one fungicidal compound selected from (b8).
    • Embodiment 25
  • A composition comprising components (a) and (b) described in the Summary of the Invention or any one of Embodiments 1 through 24 wherein component (b) comprises at least one fungicidal compound selected from (b9).
    • Embodiment 26
  • A composition comprising components (a) and (b) described in the Summary of the Invention or any one of Embodiments 1 through 25 wherein component (b) comprises at least one fungicidal compound selected from (b10).
    • Embodiment 26a
  • A composition comprising components (a) and (b) described in the Summary of the Invention or any one of Embodiments 1 through 26 wherein component (b) comprises at least one fungicidal compound selected from (b10a).
    • Embodiment 26b
  • A composition comprising components (a) and (b) described in the Summary of the Invention or any one of Embodiments 1 through 26a wherein component (b) comprises at least one fungicidal compound selected from (b10b).
    • Embodiment 27
  • A composition comprising components (a) and (b) described in the Summary of the Invention or any one of Embodiments 1 through 26b wherein component (b) comprises at least one fungicidal compound selected from (b11).
    • Embodiment 28
  • A composition comprising components (a) and (b) described in the Summary of the Invention or any one of Embodiments 1 through 27 wherein component (b) comprises at least one fungicidal compound selected from (b12).
    • Embodiment 28a
  • A composition comprising components (a) and (b) described in the Summary of the Invention or any one of Embodiments 1 through 28 wherein component (b) comprises at least one fungicidal compound selected from (b13).
    • Embodiment 29
  • A composition comprising components (a) and (b) described in the Summary of the Invention or any one of Embodiments 1 through 28a further comprising (c) least one additional compound or agent that is biologically active.
    • Embodiment 30
  • A composition of Embodiment 29 wherein component (c) comprises at least one fungicidal compound selected from the group consisting of:
      • (c1) methyl benzimidazole carbamate (MBC) fungicides;
      • (c2) dicarboximide fungicides;
      • (c3) demethylation inhibitor (DMI) fungicides;
      • (c4) phenylamide fungicides;
      • (c5) amine/morpholine fungicides;
      • (c6) phospholipid biosynthesis inhibitor fungicides;
      • (c7) carboxamide fungicides;
      • (c8) hydroxy(2-amino-)pyrimidine fungicides;
      • (c9) anilinopyrimidine fungicides;
      • (c10) N-phenyl carbamate fungicides;
      • (c11) quinone outside inhibitor (QoI) fungicides;
      • (c12) phenylpyrrole fungicides;
      • (c13) quinoline fungicides;
      • (c14) lipid peroxidation inhibitor fungicides;
      • (c15) melanin biosynthesis inhibitors-reductase (MBI-R) fungicides;
      • (c16) melanin biosynthesis inhibitors-dehydratase (MBI-D) fungicides;
      • (c17) hydroxyanilide fungicides;
      • (c18) squalene-epoxidase inhibitor fungicides;
      • (c19) polyoxin fungicides;
      • (c20) phenylurea fungicides;
      • (c21) quinone inside inhibitor (QiI) fungicides;
      • (c22) benzamide fungicides;
      • (c23) enopyranuronic acid antibiotic fungicides;
      • (c24) hexopyranosyl antibiotic fungicides;
      • (c25) glucopyranosyl antibiotic: protein synthesis fungicides;
      • (c26) glucopyranosyl antibiotic: trehalase and inositol biosynthesis fungicides;
      • (c27) cyanoacetamideoxime fungicides;
      • (c28) carbamate fungicides;
      • (c29) oxidative phosphorylation uncoupling fungicides;
      • (c30) organo tin fungicides;
      • (c31) carboxylic acid fungicides;
      • (c32) heteroaromatic fungicides;
      • (c33) phosphonate fungicides;
      • (c34) phthalamic acid fungicides;
      • (c35) benzotriazine fungicides;
      • (c36) benzene-sulfonamide fungicides;
      • (c37) pyridazinone fungicides;
      • (c38) thiophene-carboxamide fungicides;
      • (c39) pyrimidinamide fungicides;
      • (c40) carboxylic acid amide (CAA) fungicides;
      • (c41) tetracycline antibiotic fungicides;
      • (c42) thiocarbamate fungicides;
      • (c43) benzamide fungicides;
      • (c44) host plant defense induction fungicides;
      • (c45) multi-site contact activity fungicides;
      • (c46) fungicides other than fungicides of component (a) and components (c1) through (c45); and
      • salts of compounds of (c1) through (c46).
    Embodiment 31
  • A composition of Embodiment 29 or 30 wherein component (c) includes at least one compound selected from acibenzolar-S-methyl, aldimorph, ametoctradin, amisulbrom, anilazine, azaconazole, azoxystrobin, benalaxyl, benalaxyl-M, benodanil, benomyl, benthiavalicarb, benthiavalicarb-isopropyl, bethoxazin, binapacryl, biphenyl, bitertanol, bixafen, blasticidin-S, boscalid, bromuconazole, bupirimate, buthiobate, carboxin, carpropamid, captafol, captan, carbendazim, chloroneb, chlorothalonil, chlozolinate, clotrimazole, copper salts (such as Bordeaux mixture (tribasic copper sulfate), copper hydroxide and copper oxychloride), cyazofamid, cyflufenamid, cymoxanil, cyproconazole, cyprodinil, dichlofluanid, diclocymet, diclomezine, dicloran, diethofencarb, difenoconazole, diflumetorim, dimethirimol, dimethomorph, dimoxystrobin, diniconazole, diniconazole-M, dinocap, dithianon, dodemorph, dodine, edifenphos, enestroburin, epoxiconazole, etaconazole, ethaboxam, ethirimol, etridiazole, famoxadone, fenamidone, fenarimol, fenbuconazole, fenfuram, fenhexamid, fenoxanil, fenpiclonil, fenpropidin, fenpropimorph, fenpyrazamine, fentin acetate, fentin chloride, fentin hydroxide, ferbam, ferimzone, fluazinam, fludioxonil, flumetover, flumorph, fluopicolide (also known as picobenzamid), fluopyram, fluoroimide, fluoxastrobin, fluquinconazole, flusilazole, flusulfamide, flutianil (2-[[2-fluoro-5-(trifluoromethyl)phenyl]thio]-2-[3-(2-methoxyphenyl)-2-thiazolidinylidene]acetonitrile), flutolanil, flutriafol, fluxapyroxad, folpet, fosetyl-aluminum, fuberidazole, furalaxyl, furametpyr, hexaconazole, hymexazol, guazatine, imazalil, imibenconazole, iminoctadine, iodocarb, ipconazole, iprobenfos, iprodione, iprovalicarb, isoprothiolane, isopyrazam, isotianil, kasugamycin, kresoxim-methyl, mancozeb, mandipropamid, maneb, mepronil, meptyldinocap, metalaxyl, metalaxyl-M, metconazole, methasulfocarb, metiram, metominostrobin, mepanipyrim, metrafenone, myclobutanil, naftifine, neo-asozin (ferric methanearsonate), nuarimol, octhilinone, ofurace, orysastrobin, oxadixyl, oxolinic acid, oxpoconazole, oxycarboxin, oxytetracycline, penconazole, pencycuron, penflufen, penthiopyrad, pefurazoate, phosphorous acid and salts thereof, phthalide, picoxystrobin, piperalin, polyoxin, probenazole, prochloraz, procymidone, propamocarb, propamocarb-hydrochloride, propiconazole, propineb, proquinazid, prothiocarb, prothioconazole, pyraclostrobin, pyrametostrobin, pyraoxystrobin, pyrazophos, pyribencarb, pyributicarb, pyrifenox, pyrimethanil, pyriofenone, pyroquilon, pyrrolnitrin, quinconazole, quinomethionate, quinoxyfen, quintozene, sedaxane, silthiofam, simeconazole, spiroxamine, streptomycin, sulfur, tebuconazole, tebufloquin, tecloftalam, tecnazene, terbinafine, tetraconazole, thiabendazole, thifluzamide, thiophanate, thiophanate-methyl, thiram, tiadinil, tolclofos-methyl, tolylfluanid, triadimefon, triadimenol, triarimol, triazoxide, tricyclazole, tridemorph, triflumizole, tricyclazole, trifloxystrobin, triforine, trimorphamide, triticonazole, uniconazole, validamycin, valifenalate (valiphenal), vinclozolin, zineb, ziram, zoxamide, N′-[4-[4-chloro-3-(trifluoromethyl)phenoxy]-2,5-dimethylphenyl]-N-ethyl-N-methylmethanimidamide, 5-chloro-6-(2,4,6-trifluorophenyl)-7-(4-methylpiperidin-1-yl)[1,2,4]triazolo[1,5-a]pyrimidine (BAS600), N-[2-[4-[[3-(4-chlorophenyl)-2-propyn-1-yl]oxy]-3-methoxyphenyl]ethyl]-3-methyl-2-[(methylsulfonyl)amino]butanamide, N-[2-[4-[[3-(4-chlorophenyl)-2-propyn-1-yl]oxy]-3-methoxyphenyl]ethyl]-3-methyl-2-[(ethylsulfonyl)amino]butanamide, 2-butoxy-6-iodo-3-propyl-4H-1-benzopyran-4-one, 3-[5-(4-chlorophenyl)-2,3-dimethyl-3-isoxazolidinyl]pyridine, 4-fluorophenyl N-[1-[[[1-(4-cyanophenyl)ethyl]sulfonyl]methyl]propyl]carbamate, N-[[(cyclopropylmethoxy)amino][6-(difluoromethoxy)-2,3-difluorophenyl]methylene]-benzeneacetamide, α-(methoxyimino)-N-methyl-2-[[[1-[3-(trifluoromethyl)-phenyl]ethoxy]imino]methyl]benzeneacetamide, N-[4-[4-chloro-3-(trifluoro-methyl)phenoxy]-2,5-dimethylphenyl]-N-ethyl-N-methylmethanimidamide, N-(4-chloro-2-nitrophenyl)-N-ethyl-4-methylbenzenesulfonamide, 2-[[[[3-(2,6-dichlorophenyl)-1-methyl-2-propen-1-ylidene]amino]oxy]methyl]-α-(methoxyimino)-N-methylbenzeneacetamide, 1-[(2-propenylthio)carbonyl]-2-(1-methylethyl)-4-(2-methylphenyl)-5-amino-1H-pyrazol-3-one, ethyl-6-octyl-[1,2,4]triazolo[1,5-a]pyrimidin-7-ylamine, pentyl N-[4-[[[[(1-methyl-1H-tetrazol-5-yl)phenylmethylene]amino]oxy]methyl]-2-thiazolyl]carbamate, pentyl N-[6-[[[[(1-methyl-1H-tetrazol-5-yl)phenylmethylene]amino]oxy]methyl]-2-pyridinyl]carbamate, 2-[(3-bromo-6-quinolinyl)oxy]-N-(1,1-dimethyl-2-butyn-1-yl)-2-(methylthio)acetamide, 2-[(3-ethynyl-6-quinolinyl)oxy]-N-[1-(hydroxymethyl)-1-methyl-2-propyn-1-yl]-2-(methylthio)acetamide, N-(1,1-dimethyl-2-butyn-1-yl)-2-[(3-ethynyl-6-quinolinyl)oxy]-2-(methylthio)acetamide and N′-[4-[[3-[(4-chlorophenyl)methyl]-1,2,4-thiadiazol-5-yl]oxy]-2,5-dimethylphenyl]-N-ethyl-N-methylmethanimidamide.
    • Embodiment 32
  • A composition of Embodiment 31 wherein component (c) includes at least one compound selected from azoxystrobin, bixafen, boscalid (nicobifen), bromuconazole, carbendazim, chlorothalonil, cyflufenamid, cyproconazole, difenoconazole, dimoxystrobin, epoxiconazole, etaconazole, famoxadone, fenbuconazole, fenpropidin, fenpropimorph, fluopyram, flusilazole, fluxapyroxad, hexaconazole, ipconazole, isopyrazam, kresoxim-methyl, metaconazole, metominostrobin/fenominostrobin, metrafenone, myclobutanil, penconazole, penthiopyrad, picoxystrobin, prochloraz, propiconazole, proquinazid, prothioconazole, pyraclostrobin, pyrametostrobin, pyraoxystrobin, pyriofenone, quinoxyfen, sedaxane, tebuconazole, trifloxystrobin and triticonazole.
    • Embodiment 33
  • A composition of Embodiment 32 wherein component (c) includes at least one compound selected from azoxystrobin, bixafen, boscalid, cyflufenamid, cyproconazole, difenconazole, epoxiconazole, fluopyram, isopyrazam, kresoxim-methyl, metaconazole, metrafenone, myclobutanil, penthiopyrad, picoxystrobin, pyraclostrobin, pyrametrostrobin, pyraoxystrobin, pyriofenone, proquinazid, prothioconazole, quinoxyfen, sedaxane, tebuconazole and trifloxystrobin.
    • Embodiment 34
  • A composition comprising components (a) and (b) described in the Summary of the Invention or any one of Embodiments 1 through 33 wherein the composition further comprises in component (c) at least one invertebrate pest control compound or agent.
  • Of note as an embodiment is a composition comprising components (a) and (b) described in the Summary of the Invention or any one of Embodiments 1 through 34 wherein component (b1) is (b1a) (i.e. Formula B1a)
  • Figure US20150018374A1-20150115-C00016
  • Also of note is any of the fungicidal compositions or the methods relating to the compositions described in the Summary of the Invention or any embodiments described herein, including Embodiments 1-34, wherein component (b) does not comprise (b13) the compound of Formula B13, or a salt thereof. Also of note is any of the fungicidal compositions or the methods relating to the compositions described in the Summary of the Invention or any embodiments described herein, including Embodiments 1-34, wherein component (b) furthermore does not comprise (b10a) the compound of Formula B10a, (b10b) the compound of Formula B10b, or a salt thereof.
  • Embodiments of this invention, including Embodiments 1-34 above as well as any other embodiments described herein, can be combined in any manner. In addition, embodiments of this invention, including Embodiments 1-34 above as well as any other embodiments described herein, and any combination thereof, pertain to the methods of the present invention. Furthermore, embodiments of the invention described herein and their combinations pertain to compounds of Formula 1 and intermediates for their preparation, such as compounds of Formulae 14, 17, 20 and 22.
  • Of note is the composition of any one of the embodiments described herein, including Embodiments 1 through 34, wherein reference to Formula 1 includes salts thereof but not N-oxides thereof; therefore the phrase “a compound of Formula 1” can be replaced by the phrase “a compound of Formula 1 or a salt thereof”. In this composition of note, component (a) comprises a compound of Formula 1 or a salt thereof.
  • Also noteworthy as embodiments are fungicidal compositions of the present invention comprising a composition (e.g., in a fungicidally effective amount) of any one of Embodiments 1 through 34, and at least one additional component selected from the group consisting of surfactants, solid diluents and liquid diluents.
  • Embodiments of the invention further include methods for controlling plant diseases caused by fungal plant pathogens comprising applying to the plant or portion thereof, or to the plant seed or seedling, a fungicidally effective amount of a composition any one of Embodiments 1 through 34, (e.g., as a composition including formulation ingredients as described herein). Embodiments of the invention also include methods for protecting a plant or plant seed from diseases caused by fungal pathogens comprising applying a fungicidally effective amount of a composition of any one of Embodiments 1 through 34 to the plant or plant seed.
  • Some embodiments of the invention involve control of a plant disease or protection from a plant disease that primarily afflicts plant foliage and/or applying the composition of the invention to plant foliage (i.e. plants instead of seeds). The preferred methods of use include those involving the above preferred compositions; and the diseases controlled with particular effectiveness include plant diseases caused by fungal plant pathogens. Combinations of fungicides used in accordance with this invention can facilitate disease control and retard resistance development.
  • As described in the Summary of the Invention, an aspect of the present invention is directed at a composition comprising as component (a) at least one compound selected from Formula 1, N-oxides, and salts thereof. One or more of the following methods and variations as described in Schemes 1-16 can be used to prepare the compounds of Formula 1. The definitions of R1, R2, R3, R32 and M in the compounds of Formulae 1-23 below are as defined above in the Summary of the Invention unless otherwise noted. Formulae 6a and 6b are various subsets of Formula 6; Formula 10a is a subset of Formula 10; and Formula 17a is a tautomeric subset of Formula 17. Substituents for each subset formula are as defined for its parent formula unless otherwise noted.
  • As shown in Scheme 1, compounds of Formula 1 can be prepared by the reaction of 1H-pyrazole compounds of Formula 2 with various methylating agents (e.g., Formula 3), such as iodomethane, methyl sulfonates (e.g., methyl mesylate (OMs) or tosylate (OTs)) or trimethyl phosphate, preferably in the presence of an organic or inorganic base such as 1,8-diazabicyclo[5.4.0]undec-7-ene, potassium carbonate or potassium hydroxide, and in a solvent such as N,N-dimethylformamide (DMF), tetrahydrofuran (THF), toluene or water.
  • Figure US20150018374A1-20150115-C00017
  • As is shown in Scheme 2, compounds of Formula 1 can be prepared by the reaction of compounds of Formula 4 with aromatic compounds of Formula 5 containing a leaving group G (e.g., halogen or (halo)alkylsulfonate), optionally in the presence of a metal catalyst, and generally in the presence of a base and a polar aprotic solvent such as N,N-dimethylformamide or dimethyl sulfoxide. For example, compounds of Formula 5 wherein the benzene ring contains electron-withdrawing substituents react by direct displacement of the leaving group G from the ring to provide compounds of Formula 1. Compounds of Formula 5 are commercially available or their preparation is known in the art.
  • Figure US20150018374A1-20150115-C00018
  • For reactions according to the method of Scheme 2 of a compound of Formula 4 with a compound of Formula 5 wherein the aromatic ring lacks sufficiently electron-withdrawing substituents, or to improve reaction rate, yield or product purity, the use of a metal catalyst (e.g., metal or metal salt) in amounts ranging from catalytic up to superstoichiometric can facilitate the desired reaction. Typically for these conditions, G is Br or I or a sulfonate such as OS(O)2CF3 or OS(O)2(CF2)3CF3. For example, copper salt complexes (e.g., CuI with N,N-dimethylethylenediamine, proline or bipyridyl), palladium complexes (e.g., tris-(dibenzylideneacetone)dipalladium(0)) or palladium salts (e.g., palladium acetate) with ligands such as 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (i.e. “Xantphos”), 2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl (i.e. “Xphos”) or 2,2′-bis(diphenylphosphino)-1, F-binaphthalene (i.e. “BINAP”), in the presence of a base such as potassium carbonate, cesium carbonate, sodium phenoxide or sodium tert-butoxide, in a solvent such as N,N-dimethylformamide, 1,2-dimethoxyethane, dimethyl sulfoxide, 1,4-dioxane or toluene, optionally mixed with alcohols such as ethanol, can be used. Alternatively as illustrated in Scheme 3, compounds of Formula 1 can be prepared by reaction of compounds of Formula 6 (i.e. 5-bromopyrazoles or other pyrazoles substituted at the 5-position with a leaving group) with compounds of Formula 7 under metal-catalyzed conditions similar to those described above for Scheme 2. Compounds of Formula 7 are commercially available or their preparation is known in the art.
  • Figure US20150018374A1-20150115-C00019
  • As shown in Scheme 4, compounds of Formula 6 wherein G is Br or I can be prepared by reaction of 5-aminopyrazoles of Formula 4 under diazotization conditions either in the presence of, or followed by combination with, copper salts containing bromide or iodide. For example, addition of tert-butyl nitrite to a solution of a 5-aminopyrazole of Formula 4 in the presence of CuBr2 in a solvent such as acetonitrile provides the corresponding 5-bromopyrazole of Formula 6. Likewise, a 5-aminopyrazole of Formula 4 can be converted to a diazonium salt and then to a corresponding 5-halopyrazole of Formula 6 by treatment with sodium nitrite in solvents such as water, acetic acid or trifluoroacetic acid, in the presence of a mineral acid typically containing the same halide atom (such as aqueous HI solution for G being I), followed by treatment with the corresponding copper(I) or copper(II) salt according to general procedures well known to those skilled in the art.
  • Figure US20150018374A1-20150115-C00020
  • As shown in Scheme 5, 5-bromopyrazoles of Formula 6a (i.e. Formula 6 wherein G is Br) can be prepared by reacting 5-hydroxypyrazoles of Formula 8 with phosphorus tribromide as described in Tetrahedron Lett. 2000, 41(24), 4713.
  • Figure US20150018374A1-20150115-C00021
  • As shown in Scheme 6, 5-hydroxypyrazoles of Formula 8 can also be used to prepare 5-fluoroalkylsulfonyl (e.g., 5-trifluoromethanesulfonyl, 5-nonafluorobutylsulfonyl) pyrazoles of Formula 6b (i.e. Formula 6 wherein G is fluoroalkylsulfonyloxy) as described in Synlett 2004, 5, 795.
  • Figure US20150018374A1-20150115-C00022
  • As shown in Scheme 7, compounds of Formula 1 can be prepared by reaction of 4-bromo or iodo pyrazoles of Formula 9 with organometallic compounds of Formula 10 under transition-metal-catalyzed cross-coupling reaction conditions. Reaction of a 4-bromo or iodo pyrazole of Formula 9 with a boronic acid, trialkyltin, zinc or organomagnesium reagent of Formula 10 in the presence of a palladium or nickel catalyst having appropriate ligands (e.g., triphenylphosphine (PPh3), dibenzylideneacetone (dba), dicyclohexyl(2′,6′-dimethoxy[1,1′-biphenyl]-2-yl)phosphine (SPhos)) and a base, if needed, affords the corresponding compound of Formula 1. For example, a substituted aryl boronic acid or derivative e.g., Formula 10 wherein M is B(OH)2, B(OC(CH3)2C(CH3)2O)) or B(O-i-Pr)3 ⊖Li⊕, reacts with a 4-bromo- or 4-iodopyrazole of Formula 9 in the presence of dichlorobis(triphenylphosphine) palladium(II) and aqueous base such as sodium carbonate or potassium hydroxide, in solvents such as 1,4-dioxane, 1,2-dimethoxyethane, toluene or ethyl alcohol, or under anhydrous conditions with a ligand such as phosphine oxide or phosphite ligand (e.g., diphenylphosphine oxide) and potassium fluoride in a solvent such as 1,4-dioxane (see Angewandte Chemie, International Edition 2008, 47(25), 4695-4698) to provide the corresponding compound of Formula 1.
  • Figure US20150018374A1-20150115-C00023
  • As illustrated in Scheme 8, compounds of Formula 4 can be prepared by reacting compounds of Formula 11 with compounds of Formula 10a (e.g., compounds of Formula 10 wherein M is B(OH)2) using transition-metal-catalyzed cross-coupling reaction conditions as described for the method of Scheme 7.
  • Figure US20150018374A1-20150115-C00024
  • As illustrated in Scheme 9, pyrazoles of Formula 9 wherein G is Br or I are readily prepared by the reaction of pyrazoles unsubstituted at the 4-position (Formula 12) with halogenating reagents such as bromine, sodium bromite, N-bromosuccinimide (NBS) or N-iodosuccinimide (NIS), in solvents such as acetic acid, acetonitrile, N,N-dimethylformamide, N,N-dimethylacetamide or 1,4-dioxane, or a mixture of water with the aforementioned solvents, at temperatures ranging from ambient to the boiling point of the solvent.
  • Figure US20150018374A1-20150115-C00025
  • As illustrated in Scheme 10, using reaction conditions similar to those for the method of Scheme 9, the pyrazole of Formula 13 can be converted into intermediates of Formula 11 which are useful for preparing compounds of Formula 4 as depicted in Scheme 8. The compound of Formula 13 not only can be prepared by methods known in the art, but is also commercially available.
  • Figure US20150018374A1-20150115-C00026
  • As shown in Scheme 11, compounds of Formula 12 can be prepared from corresponding compounds of Formula 13 by procedures analogous to those used for the method of Scheme 2. Compounds of Formula 13 are commercially available or can be prepared by methods known in the art.
  • Figure US20150018374A1-20150115-C00027
  • General methods useful for preparing 5-aminopyrazoles of Formula 4 are well known in the art; see, for example, Journal für Praktische Chemie (Leipzig) 1911, 83, 171 and J. Am. Chem. Soc. 1954, 76, 501. Such a method is illustrated in Scheme 12.
  • Figure US20150018374A1-20150115-C00028
  • Similarly, general methods useful for preparing 5-hydroxypyrazoles of Formula 8 are well known in the art; see, for example, Annalen der Chemie 1924, 436, 88. Such a method is illustrated in Scheme 13.
  • Figure US20150018374A1-20150115-C00029
  • As shown in Scheme 14, compounds of Formula 1 can be prepared by condensing compounds of Formula 17 with methylhydrazine (Formula 15) in a solvent such as ethanol or methanol and optionally in the presence of an acid or base catalyst such as acetic acid, piperidine or sodium methoxide, according to general procedures known in the art. The method of Scheme 14 is illustrated by Step C of Synthesis Example 1 and Step B of Synthesis Example 2.
  • Figure US20150018374A1-20150115-C00030
  • In a manner analogous to the method of Scheme 14, compounds of Formula 2 can be similarly prepared by condensing compounds of Formula 17 with hydrazine. This method is described in Chemistry of Heterocyclic Compounds 2005, 41(1), 105-110.
  • As shown in Scheme 15, compounds of Formula 17 (wherein, R32 is H or lower alkyl such as CH3, CH2CH3 or (CH2)2CH3) can be prepared by reaction of corresponding ketene dithioacetal compounds of Formula 18 with compounds of Formula 19 optionally in the presence of a base, such as sodium hydride or ethylmagnesium chloride, in solvents such as toluene, tetrahydrofuran or dimethoxymethane, at temperatures ranging from −10° C. to the boiling point of the solvent. See, for example, J. Heterocycl. Chem. 1975, 12(1), 139. Methods useful for preparing compounds of Formula 18 are known in the art.
  • Figure US20150018374A1-20150115-C00031
  • As shown in Scheme 16, compounds of Formula 17 wherein R32 is lower alkyl (e.g., methyl, ethyl, n-propyl) and Formula 17a (i.e. tautomer of Formula 17 wherein R32 is H) can be prepared starting by condensation reaction of corresponding isothiocyanate compounds of Formula 20 with arylacetone compounds of Formula 21 to give intermediate compounds of Formula 22, which are salts of the thioamides of Formula 17a. The intermediate compounds of Formula 22 can either be used in situ as is illustrated by Step C of Synthesis Example 1 or isolated before further conversion as is illustrated by Steps A and B of Synthesis Example 2. Bases useful for preparing compounds of Formula 22 include hydrides, alkoxides, hydroxides or carbonates of sodium or potassium, such as sodium hydride, potassium tert-butoxide, sodium ethoxide, potassium hydroxide, sodium hydroxide or potassium carbonate. Amine bases (e.g., triethylamine or N,N-diisopropylethylamine) can also be used to effect the condensation of the compounds of Formulae 20 and 21. A variety of solvents are useful, such as tetrahydrofuran, ether, toluene, N,N-dimethylformamide, alcohols (e.g., ethanol), esters (e.g., ethyl acetate or isopropyl acetate), or mixtures thereof. Solvents are chosen for compatibility with the base selected, as is well-known in the art. Reaction temperatures can range from −78° C. to the boiling point of the solvent. One useful mixture of base and solvent is potassium tert-butoxide in tetrahydrofuran, to which at −70 to 0° C. is added a solution of an isothiocyanate of Formula 20 and a carbonyl compound of Formula 21, which are either combined into one solution, or added separately, preferably by addition of the carbonyl compound followed by addition of the isothiocyanate. The salt compound of Formula 22 can be acidified to form the ketothioamide compound of Formula 17a or alkylated with R32X1 (Formula 23) wherein R32 is lower alkyl (e.g., methyl, ethyl, n-propyl) and X1 is a nucleofuge (i.e. a nucleophilic reaction leaving group such as Br, I, OS(O)2CH3) to form the corresponding compound of Formula 17. This general method is known in the chemical literature; see, for example, Zhurnal Organicheskoi Khimii 1982, 18(12), 2501. The method of Scheme 16 to prepare a non-isolated intermediate compound of Formula 17 wherein R32 is methyl is illustrated by Step C of Synthesis Example 1. The method of Scheme 16 to prepare an isolated intermediate compound of Formula 22 is illustrated by Step A of Synthesis Example 2.
  • Figure US20150018374A1-20150115-C00032
  • Ketothioamides of Formula 17a can also be prepared by allowing the corresponding ketoamides to react with sulfurizing agents such as Lawesson's reagent or P2S5; see, for example, Helv. Chim. Act. 1998, 81(7), 1207.
  • It is recognized by one skilled in the art that various functional groups can be converted into others to provide different compounds of Formula 1. For example, intermediates for the preparation of compounds of Formula 1 may contain aromatic nitro groups, which can be reduced to amino groups, and then be converted via reactions well known in the art such as the Sandmeyer reaction, to various halides, providing compounds of Formula 1.
  • The above reactions can also in many cases be performed in alternate sequence, such as the preparation of 1H pyrazoles for use in the reaction in Scheme 2 by reactions illustrated later for the general preparation of substituted pyrazoles.
  • It is recognized that some reagents and reaction conditions described above for preparing compounds of Formula 1 may not be compatible with certain functionalities present in the intermediates. In these instances, the incorporation of protection/deprotection sequences or functional group interconversions into the synthesis will aid in obtaining the desired products. The use and choice of the protecting groups will be apparent to one skilled in chemical synthesis (see, for example, Greene, T. W.; Wuts, P. G. M. Protective Groups in Organic Synthesis, 2nd ed.; Wiley: New York, 1991). One skilled in the art will recognize that, in some cases, after the introduction of a given reagent as it is depicted in any individual scheme, it may be necessary to perform additional routine synthetic steps not described in detail to complete the synthesis of compounds of Formula 1. One skilled in the art will also recognize that it may be necessary to perform a combination of the steps illustrated in the above schemes in an order other than that implied by the particular sequence presented to prepare the compounds of Formula 1. One skilled in the art will also recognize that compounds of Formula 1 and the intermediates described herein can be subjected to various electrophilic, nucleophilic, radical, organometallic, oxidation, and reduction reactions to add substituents or modify existing substituents.
  • Without further elaboration, it is believed that one skilled in the art using the preceding synthesis description can utilize the present invention to its fullest extent. The following Synthesis Examples are, therefore, to be construed as merely illustrative, and not limiting of the disclosure in any way whatsoever. Steps in the following Synthesis Examples illustrate a procedure for each step in an overall synthetic transformation, and the starting material for each step may not have necessarily been prepared by a particular preparative run whose procedure is described in other Steps. Percentages are by weight except for chromatographic solvent mixtures or where otherwise indicated. Parts and percentages for chromatographic solvent mixtures are by volume unless otherwise indicated. 1H NMR spectra are reported in ppm downfield from tetramethylsilane in CDCl3 unless otherwise noted; “s” means singlet, “br s” means broad singlet, “d” means doublet, “dd” means doublet of doublets, “t” means triplet, “dt” means doublet of triplets, “m” means multiplet.
    • Synthesis Example 1 Preparation of 4-(2-Bromo-4-fluorophenyl)-N-(2-chloro-6-fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine (Compound 4) Step A: Preparation of 1-(2-Bromo-4-fluorophenyl)-2-propanone
  • A solution of sodium methoxide in methanol (25%, 34 mL, 157 mmol) was combined with toluene (200 mL). The methanol was then distilled off at 90° C. using a Dean-Stark trap. After the solution was cooled to 70° C., 2-bromo-4-fluorobenzeneacetonitrile (21.4 g, 100 mmol) dissolved in ethyl acetate (40 mL) was added from a dropping funnel over 20 min with mechanical stirring. At this point additional toluene (150 mL) was added to facilitate stirring of a voluminous light pink precipitate. The reaction mixture was poured into water, and the organic phase was separated. The aqueous phase was acidified and extracted with ethyl acetate. The ethyl acetate phase was dried and concentrated under reduced pressure to provide the intermediate compound α-acetyl-2-bromo-4-fluorobenzeneacetonitrile as a crude oil.
  • The crude oil was stirred in sulfuric acid (60%, 170 mL), and the resulting mixture was refluxed for 6.5 h. The reaction mixture was then extracted with hexanes (2×100 mL), and the combined hexane extracts were washed with water and brine, dried (MgSO4) and concentrated under reduced pressure to yield the title compound as a yellow oil (14.7 g), which was used without further purification in Step C.
  • 1H NMR δ 7.33 (m, 1H), 7.18 (m, 1H), 7.01 (m, 1H), 3.85 (s, 2H), 2.23 (s, 3H).
    • Step B: Preparation of 1-Chloro-3-fluoro-2-isothiocyanatobenzene
  • To a solution of 2-chloro-6-fluorobenzenamine (5.0 g, 34 mmol) in chlorobenzene (52 mL) was added carbonothioic dichloride (thiophosgene) (5.1 g, 45 mmol) and DMF (0.27 mL). The reaction mixture was refluxed for 2 h and then concentrated to leave the title compound as a brown oil (6.15 g), which was used in Step C without further purification.
  • 1H NMR δ 7.18 (m, 2H), 7.07 (m, 1H).
    • Step C: Preparation of 4-(2-Bromo-4-fluorophenyl)-N-(2-chloro-6-fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine
  • To a solution of potassium tert-butoxide (0.41 g, 3.3 mmol) in THF (20 mL) at 0° C. was added a solution of 1-(2-bromo-4-fluorophenyl)-2-propanone (i.e. the product of Step A) (0.70 g, 3.0 mmol) in THF (10 mL) over 5 minutes. Stirring was continued for 1 h and then the temperature was reduced to −10° C. A solution of 1-chloro-3-fluoro-2-isothiocyanatobenzene (i.e. the product of Step B) (0.57 g, 3.0 mmol) in THF (10 mL) was added over 6 minutes, and stirring was continued for 15 minutes to provide a reaction mixture containing the intermediate compound 3-(2-bromo-4-fluorophenyl)-4-[(2-chloro-6-fluorophenyl)amino]-4-mercapto-3-buten-2-one potassium salt (1:1), which is the potassium salt of α-acetyl-2-bromo-N-(2-chloro-6-fluorophenyl)-4-fluorobenzeneethanethioamide. Iodomethane (0.54 g, 3.8 mmol) was added, and the cooling bath was removed to provide a reaction mixture containing the intermediate compound 3-(2-bromo-4-fluorophenyl)-4-[(2-chloro-6-fluorophenyl)amino]-4-(methylthio)-3-buten-2-one. After 5 min, water (0.2 mL, 11 mmol), glacial acetic acid (0.53 mL, 9.1 mmol) and methylhydrazine (0.81 mL, 15 mmol) were added in rapid succession, and the reaction mixture was heated to reflux for 6 h. The crude reaction mixture was then concentrated under reduced pressure and purified by MPLC (0 to 100% ethyl acetate in hexanes as eluent) to provide the title product as an off-white solid (0.55 g).
  • 1H NMR δ 7.24 (m, 1H), 7.04 (m, 1H), 6.95 (m, 1H), 6.87 (m, 1H), 6.78 (m, 1H), 6.68 (m, 1H), 5.45 (d, 1H), 3.80 (s, 3H), 2.10 (s, 3H).
    • Example 2 Preparation of 4-(2-Bromo-4-fluorophenyl)-N-(2,6-difluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine (Compound 11) Step A: Preparation of 3-(2-Bromo-4-fluorophenyl)-4-[(2,6-difluorophenyl)amino]-4-mercapto-3-buten-2-one potassium salt (1:1)
  • To a solution of 1-(2-bromo-4-fluorophenyl)-2-propanone (23.4 g, 101 mmol) in methyl tert-butyl ether (300 mL) cooled to 6° C. with aid of an ice bath was added a tetrahydrofuran solution of potassium tert-butoxide (1.0 M, 100 mL, 100 mmol) over 30 min During the addition of about 90 mL of potassium tert-butoxide solution the temperature of the reaction mixture was maintained at 6-8° C., and then the ice bath was removed during the addition of the remaining potassium tert-butoxide solution.
  • At the completion of the potassium tert-butoxide solution addition, the reaction mixture was a light yellow solution at 12° C. The reaction mixture was stirred for 30 min at 12-16° C. The reaction mixture was then cooled to 3° C., and a solution of 1,3-difluoro-2-isothiocyanatobenzene (17.4 g, 102 mmol) in methyl tert-butyl ether (50 mL) was added over 20 min while maintaining the temperature of the reaction mixture between 3 and 5° C. The resulting yellow slurry was then slowly warmed to 12° C. over 90 min. The mixture was diluted with hexanes (100 mL) and cooled to 8° C., and then the solid product was isolated by filtration. The product was dried in a vacuum oven at 70° C. overnight to provide the title product as a yellow solid (32.3 g).
  • 1H NMR (DMSO-d6) δ 14.36 (s, 1H), 7.38 (dd, 1H), 7.22 (dd, 1H), 7.17 (m, 1H), 7.06 (dd, 1H), 6.99 (t, 2H), 1.50 (s, 3H).
    • Step B: Preparation of 4-(2-Bromo-4-fluorophenyl)-N-(2,6-difluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine
  • A stirred mixture of 3-(2-bromo-4-fluorophenyl)-4-[(2,6-difluorophenyl)amino]-4-mercapto-3-buten-2-one potassium salt (1:1) (i.e. the product of Step A) (32.3 g, 73.4 mmol), acetic acid (44 g, 73 mmol) and methylhydrazine (109 mmol) in ethanol (200 mL) was heated at 65° C. for 3 h. Then the temperature was increased to 70° C. over 15 min To the light yellow cloudy reaction mixture was added water (200 mL) over 30 min. The resulting yellow slurry was cooled to 8° C. over 2 h and then held at 8° C. for 30 min more. The solids were collected by filtration, rinsed with aqueous ethanol (1:4 EtOH—H2O by volume) and dried in a vacuum oven at 70° C. to provide the title product as yellow solid (25 g).
  • 1H NMR δ 7.23 (dd, 1H), 7.06 (dd, 1H), 6.89 (dt, 1H), 6.68 (m, 3H), 5.15 (br s, 1H), 3.81 (s, 3H), 2.11 (s, 3H).
  • By the procedures described herein together with methods known in the art, the compounds disclosed in Table 1 that follows can be prepared.
  • TABLE 1
    Figure US20150018374A1-20150115-C00033
    R1 R2 R3
    F H Cl
    Cl H Cl
    Br H Cl
    F H Br
    Cl H Br
    Br H Br
    F F Cl
    Cl F Cl
    Br F Cl
    F F Br
    Cl F Br
    Br F Br
  • Tables 2-5 disclose specific compounds useful as process intermediates for preparing compounds of Formula 1, N-oxides, and salts thereof. The “Note” column in these tables references physical property data (e.g., 1H NMR spectra, MS parent ion(s), melting ranges) for representative compounds. Mass spectra (MS) are reported as the molecular weight of the highest isotopic abundance parent ion (M+1) formed by addition of H+ (molecular weight of 1) to the molecule, observed by mass spectrometry using atmospheric pressure chemical ionization (AP+). The presence of molecular ions containing one or more higher atomic weight isotopes of lower abundance (e.g., 37Cl, 81Br) is not reported. In some instances, the M−1 ion is also reported.
  • As described for Scheme 12, compounds of Formula 14 are useful process intermediates for preparing compounds of Formula 4 as intermediates to compounds of Formula 1, which are useful as component (a) in the present composition. Illustrative of compounds of Formula 14 are those specifically disclosed in Table 2.
  • TABLE 2
    14
    Figure US20150018374A1-20150115-C00034
    R3 Note
    Cl 2-1
    Br 2-2
    Note 2-1: 1H NMR (CDCl3) δ 7.49 (m, 1H), 7.25 (m, 1H), 7.11 (m, 1H), 5.14 (s,
    1H), 2.36 (s, 3H).
    Note 2-2: 1H NMR (CDCl3) δ 7.49 (m, 2H), 7.41 (m, 1H), 7.17 (m, 1H), 5.20 (s,
    1H), 2.35 (s, 3H).
  • As described for Scheme 14, compounds of Formula 17 including Formula 17a (Formula 17 tautomer wherein R32 is H) are useful process intermediates for preparing compounds of Formula 1, which are useful as component (a) in the present composition. Illustrative of compounds of Formulae 17 and 17a are those specifically disclosed in Table 3a and 3b.
  • TABLE 3a
    Figure US20150018374A1-20150115-C00035
    R1 R2 R3 Note
    F H Cl
    Cl H Cl
    Br H Cl
    F H Br
    Cl H Br 3a-1
    Br H Br
    F F Cl
    Cl F Cl
    Br F Cl 3a-2
    F F Br 3a-3
    Cl F Br
    Br F Br
    Note 3a-1: 1H NMR (CDCl3) δ 15.36 (s, 1H), 8.09 (d, 1H), 7.62 (br s, 1H), 7.52 (dd,
    1H), 7.42 (q, 1H), 7.37 (d, 1H), 7.29 (t, 1H), 7.19 (m, 2H), 1.82 (s, 3H).
    Note 3a-2: MS 420 (M + 1). Melting 134-135° C.
    Note 3a-3: 1H NMR (CDCl3) δ 15.29 (s, 1H), 7.53 (dd, 1H), 7.43 (dd, 1H), 7.29 (m,
    1H), 7.19 (dt, 1H), 6.95 (t, 2H), 6.82 (s, 1H), 1.81 (s, 3H).
  • TABLE 3b
    17
    Figure US20150018374A1-20150115-C00036
    R1 R2 R3 Note
    R32 is CH3.
    F H Cl
    Cl H Cl 3b-1
    Br H Cl 3b-2
    F F Cl 3b-3
    Cl F Cl
    Br F Cl 3b-4
    F F Br 3b-5
    Cl F Br 3b-6
    Br F Br 3b-7
    R32 CH2CH3.
    F H Cl
    Cl H Cl
    Br H Cl
    F H Br
    Cl H Br
    Br H Br
    F F Cl
    Cl F Cl
    Br F Cl
    F F Br
    Cl F Br
    Br F Br
    R32 is (CH2)2CH3.
    F H Cl
    Cl H Cl
    Br H Cl
    F H Br
    Cl H Br
    Br H Br
    F F Cl
    Cl F Cl
    Br F Cl
    F F Br
    Cl F Br
    Br F Br
    Note 3b-1: 1H NMR (CDCl3) δ 12.76 (s, 1H), 766 (d, 1H), 7.43 (m, 2H), 7.32 (q,
    1H), 7.24 (t, 1H), 7.10 (m, 2H), 1.89 (s, 3H), 1.84 (s, 3H).
    Note 3b-2: MS 459.8 (M + 1), 457.9 (M − 1).
    Note 3b-3: MS 372.0 (M + 1).
    Note 3b-4: MS 433.8 (M + 1).
    Note 3b-5: 1H NMR (CDCl3) δ 12.53 (s, 1H), 7.42 (dd, 1H), 7.32 (dd, 1H), 7.22 (m,
    1H), 7.08 (dt, 1H), 6.97 (t, 2H), 1.92 (s, 3H), 1.89 (s, 3H).
    Note 3b-6: MS 433.8 (M + 1), 431.8 (M − 1).
    Note 3b-7: MS 477.8 (M + 1), 475.8 (M − 1).
  • As described for Scheme 16, compounds of Formula 20 are useful process intermediates for preparing compounds of Formulae 17 and 17a as intermediates to compounds of Formula 1, which are useful as component (a) in the present composition. Illustrative of compounds of Formula 20 are those specifically disclosed in Table 4.
  • TABLE 4
    20
    Figure US20150018374A1-20150115-C00037
    R1 R2 Note
    F H
    Cl H
    Br H
    F F
    Cl F 4-1
    Br F 4-2
    Note 4-1: See Synthesis Example 1, Step B for 1H NMR spectrum.
    Note 4-2: 1H NMR (CDCl3) δ 7.36 (m, 1H), 7.10 (m, 1H). 19F NMR (CDCl3) δ
    −114.93 (m, 1F).
  • As described for Scheme 16, compounds of Formula 22 are useful process intermediates for preparing compounds of Formulae 17 and 17a as intermediates to compounds of Formula 1, which are useful as component (a) in the present composition. Illustrative of compounds of Formula 22 are those specifically disclosed in Table 5.
  • TABLE 5
    22
    Figure US20150018374A1-20150115-C00038
    R1 R2 R3 Note
    M is Na.
    F H Cl
    Cl H Cl
    Br H Cl 5-1
    F H Br
    Cl H Br
    Br H Br
    F F Cl
    Cl F Cl
    Br F Cl
    F F Br
    Cl F Br
    Br F Br
    M is K.
    F H Cl
    Cl H Cl
    Br H Cl
    F H Br
    Cl H Br 5-2
    Br H Br
    F F Cl
    Cl F Cl
    Br F Cl
    F F Br 5-3
    Cl F Br
    Br F Br
    Note 5-1: Melting 115-118° C.
    Note 5-2: 1H NMR (DMSO-d6) δ 15.09 (s, 1H), 8.98 (d, 1H), 7.39 (d, 1H),
    7.35 (d, 1H), 7.21 (dd, 1H), 7.10 (m, 2H), 6.90 (t, 1H), 1.49 (s, 3H).
    Note 5-3: See Synthesis Example 2, Step B for 1H NMR spectrum.
  • Remarkably, 2,6-substituted aniline-pyrazole compounds of Formula 1 have now been discovered to have significantly improved pharmacokinetic properties compared to corresponding compounds wherein the phenyl ring connected to R1 and R2 has a nonhydrogen substituent at the para position relative to the bond connecting the phenyl ring to the remainder of the molecule. In particular in vertebrate animals, compounds of Formula 1 compared to para-substituted analogs have been found to have a significantly diminished distribution into fat, thereby reducing the possibility of bioaccumulation. Furthermore, in addition to having more favorable pharmacokinetic properties in vertebrate animals, 2,6-substituted anilino-pyrazole compounds of Formula 1 wherein R2 is F, have been discovered to retain remarkably high activity when the phenyl para position is unsubstituted against plant fungal diseases, such as caused by Septoria tritici. Because of their extraordinarily desirable biological profile, compounds of Formula 1 are remarkably useful as component (a) in combination with fungicidal compounds of component (b) and optionally other biologically active compounds or agents as component (c) in the present compositions. Moreover, process intermediates useful for preparing compounds of Formula 1, such as compounds of Formulae 14, 17, 20 and 22 are correspondingly particularly useful.
  • The pharmacokinetic properties of compounds of Formula 1 can be measured using a wide variety of assay protocols known in the science of pharmacology. In one illustrative method involving a single oral dose, three male and three female rats receive a single dose of a test substance via oral gavage. Approximately 0.25 mL of blood is collected via tail vein immediately prior to dosing, and then at 0.25, 0.5, 1, 2, 4, 8, 12, 24 h and every 24 h thereafter until sacrifice. At sacrifice, fat is also collected to determine the fat:plasma ratio at sacrifice. Blood is collected into tubes that contain ethylenediaminetetracetic acid (EDTA) and centrifuged at 2500×g in order to separate plasma from blood cells. The plasma is then extracted by protein precipitation using, for example, acetonitrile and a protein precipitation plate (e.g., Strata Impact Protein Precipitation Plate, part number CEO-7565 of Phenomenex, Torrance, Calif., U.S.A.) following directions provided for the plate. Alternatively, the plasma is extracted just with acetonitrile, vortexed (i.e. mixed using a vortex mixer), and centrifuged to pellet the proteins. After removal of the proteins, the plasma is analyzed for parent compound and/or metabolites by liquid chromatography-mass spectrometry (LC/MS). The fat is homogenized and extracted by an organic solvent such as acetonitrile. The extract is then analyzed for parent compound and/or metabolites by LC/MS. The plasma pharmacokinetic data is then analyzed using nonlinear modeling software (e.g., WinNonlin™ from Pharsight, Cary, N.C., U.S.A.) to determine half-life of the administered compound in plasma, the time after administration when the maximum plasma concentration is reached (Tmax), the maximum plasma concentration (Cmax) and the area under the plasma concentration curve (AUC). As analysis of fat requires rat sacrifice, fat data is obtained at single time points (i.e. the time of rat sacrifice). However, by using multiple rats sacrificed after different intervals from time of dosing, such parameters as Cmax for fat are determined Using the above described method, Compounds 3, 4 and 5 identified in Index Table A are found to have a significantly diminished distribution into fat compared to corresponding compounds wherein the phenyl ring connected to R1 and R2 has a nonhydrogen substituent at the para position relative to the bond connecting the phenyl ring to the remainder of the molecule.
  • In a composition comprising (a) at least one compound selected from Formula 1, N-oxides, and salts thereof, with (b) at least one fungicidal compound selected from component (b), component (b) is selected from components (b1) through (b13), i.e. Formulae B1 through B13, respectively, including salts thereof.
  • Component (b1) relates to the compound of Formula B1
  • Figure US20150018374A1-20150115-C00039
  • wherein Rb20 and Rb21 are independently CH3, CF2H or CF3; each Rb22 is independently halogen or cyano; n is 0, 1, 2 or 3; and L is a direct bond or —CH2O— wherein the left bond is connected to the dihydroisoxazole ring and the right bond is connected to the phenyl ring. Of note as an example of a compound of Formula B1 wherein L is a direct bond is (b1a) the compound of Formula B1a
  • Figure US20150018374A1-20150115-C00040
  • which is 1-[4-[4-[5-(2,6-difluorophenyl)-4,5-dihydro-3-isoxazolyl]-2-thiazolyl]-1-piperidinyl]-2-[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]ethanone (Registry Number 1003318-67-9). Of particular note is (b1aa) the R enantiomer of Formula B1a-R
  • Figure US20150018374A1-20150115-C00041
  • which is 1-[4-[4-[5R-(2,6-difluorophenyl)-4,5-dihydro-3-isoxazolyl]-2-thiazolyl]-1-piperidinyl]-2-[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]ethanone (Registry Number 1003319-79-6). Examples of a compound of Formula B1 wherein L is —CH2O— include (b1b) the compound of Formula B1b
  • Figure US20150018374A1-20150115-C00042
  • which is 1-[4-[4-[5-[(2,6-difluorophenoxy)methyl]-4,5-dihydro-3-isoxazolyl]-2-thiazolyl]-1-piperdinyl-2-[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]ethanone. Methods for preparing compounds of Formula B1 are described in PCT Patent Publication WO 2008/013622 and PCT Patent Application PCT/US11/64324.
  • Component (b2) relates to a compound of Formula B2
  • Figure US20150018374A1-20150115-C00043
      • wherein Rb1 is
  • Figure US20150018374A1-20150115-C00044
  • Examples of a compound of Formula B2 include (b2a) (2-chloro-6-fluorophenyl)methyl 2-[1-[2-[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]acetyl]-4-piperidinyl]-4-thiazolecarboxylate (Registry Number 1299409-40-7) and (b2b) (1R)-1,2,3,4-tetrahydro-1-naphthalenyl 2-[1-[2-[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]acetyl]-4-piperidinyl]-4-thiazolecarboxylate (Registry Number 1299409-42-9). Methods for preparing compounds of Formula B2 are described in PCT Patent Publications WO 2009/132785 and WO 2011/051243.
  • Component (b3) relates to a compound of Formula B3
  • Figure US20150018374A1-20150115-C00045
      • wherein Rb2 is —CH2OC(O)CH(CH3)2, —C(O)CH3, —CH2OC(O)CH3, —C(O)OCH2CH(CH3)2 or
  • Figure US20150018374A1-20150115-C00046
  • Examples of a compound of Formula B3 include (b3a) [[4-methoxy-2-[[[(3S,7R,8R,9S)-9-methyl-8-(2-methyl-1-oxopropoxy)-2,6-dioxo-7-(phenylmethyl)-1,5-dioxonan-3-yl]-amino]carbonyl]-3-pyridinyl]oxy]methyl 2-methylpropanoate (Registry Number 517875-34-2), (b3b) (3S,6S,7R,8R)-3-[[[3-(acetyloxy)-4-methoxy-2-pyridinyl]carbonyl]amino]-6-methyl-4,9-dioxo-8-(phenylmethyl)-1,5-dioxonan-7-yl 2-methylpropanoate (Registry Number 234112-93-7), (b3c) (3S,6S,7R,8R)-3-[[[3-[(acetyloxy)methoxy]-4-methoxy-2-pyridinyl]carbonyl]amino]-6-methyl-4,9-dioxo-8-(phenylmethyl)-1,5-dioxonan-7-yl 2-methylpropanoate (Registry Number 517875-31-9), (b3d) (3S,6S,7R,8R)-3-[[[4-methoxy-3-[[(2-methylpropoxy)carbonyl]oxy]-2-pyridinyl]carbonyl]amino]-6-methyl-4,9-dioxo-8-(phenylmethyl)-1,5-dioxonan-7-yl 2-methylpropanoate (Registry Number 328256-72-0), and (b3e) N-[[3-(1,3-benzodioxol-5-ylmethoxy)-4-methoxy-2-pyridinyl]carbonyl]-O-[2,5-dideoxy-3-O-(2-methyl-1-oxopropyl)-2-(phenylmethyl)-L-arabinonoyl]-L-serine, (1→4′)-lactone (Registry Number 1285706-70-8). Methods for preparing compounds of Formula B3 are described in PCT Patent Publications WO 99/40081, WO 2001/014339, WO 2003/035617 and WO 2011044213.
  • Component (b4) relates to a compound of Formula B4
  • Figure US20150018374A1-20150115-C00047
  • wherein Rb3 is CH3 or F.
  • Examples of a compound of Formula B4 include (b4a) 5-fluoro-2-[(4-methylphenyl)-methoxy]-4-pyrimidinamine (Registry Number 1174376-25-0) and (b4b) 5-fluoro-2-[(4-fluorophenyl)methoxy]-4-pyrimidinamine (Registry Number 1174376-11-4). Compounds of Formula B4 can be prepared by methods described in PCT Patent Publication WO 2009/094442.
  • Component (b5) relates to the compound of Formula B5
  • Figure US20150018374A1-20150115-C00048
  • which is 5,8-difluoro-N-[2-[3-methoxy-4-[[4-(trifluoromethyl)-2-pyridinyl]oxy]phenyl]-ethyl]-4-quinazolinamine (Registry Number 1210070-31-7). The compound of Formula B5 can be prepared by methods described in PCT Patent Publication WO 2010/025451.
  • Component (b6) relates to a compound of Formula B6
  • Figure US20150018374A1-20150115-C00049
  • wherein Rb4 is —(CH2)4CH3, —C(CH3)3 or —(CH2)2C≡CH.
  • Examples of a compound of Formula B6 include (b6a) pentyl[6-[[[(Z)-[(1-methyl-1H-tetrazol-5-yl)phenylmethylene]amino]oxy]methyl]-2-pyridinyl]carbamate (Registry Number 500207-05-6), (b6b) 1,1-dimethylethyl N-[6-[[[(Z)-[(1-methyl-1H-tetrazol-5-yl)-phenylmethylene]amino]oxy]methyl]-2-pyridinyl]carbamate (Registry Number 500207-04-5), and (b6c) 3-butyn-1-yl N-[6-[[[(Z)-[(1-methyl-1H-tetrazol-5-yl)phenylmethylene]amino]-oxy]methyl]-2-pyridinyl]carbamate (Registry Number 1202946-82-4). Compounds of Formula B6 can be prepared by methods described in PCT Patent Publication WO 2003/016303.
  • Component (b7) relates to the compound of Formula B7
  • Figure US20150018374A1-20150115-C00050
  • which is N-(3′,4′-difluoro[1,1′-biphenyl]-2-yl)-3-(trifluoromethyl)-2-pyrazinecarboxamide (Registry Number 942515-63-1). The compound of Formula B7 can be prepared by methods described in PCT Patent Publication WO 2007/072999.
  • Component (b8) relates to the compound of Formula B8
  • Figure US20150018374A1-20150115-C00051
  • which is N-[2-(2,4-dichlorophenyl)-2-methoxy-1-methylethyl]-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxamide (Registry Number 1092400-95-7). The compound of Formula B8 can be prepared by methods described in PCT Patent Publication WO 2008/148570.
  • Component (b9) relates to a compound of Formula B9
  • Figure US20150018374A1-20150115-C00052
  • wherein Rb5 is H or F, and Rb6 is —CF2CHFCF3 or —CF2CF2H. Examples of a compound of Formula B9 are (b9a) 3-(difluoromethyl)-N-[4-fluoro-2-(1,1,2,3,3,3-hexafluoropropoxy)-phenyl]-1-methyl-1H-pyrazole-4-carboxamide (Registry Number 1172611-40-3) and (b9b) 3-(difluoromethyl)-1-methyl-N-[2-(1,1,2,2-tetrafluoroethoxy)phenyl]-1H-pyrazole-4-carboxamide (Registry Number 923953-98-4). Compounds of Formula B9 can be prepared by methods described in PCT Patent Publication WO 2007/017450.
  • Component (b10) relates to a compound of Formula B10
  • Figure US20150018374A1-20150115-C00053
  • wherein
    • Rb7 is
  • Figure US20150018374A1-20150115-C00054
  • Rb8 is H, halogen or C1-C2 alkyl;
    Rb9 is C1-C8 alkyl, C1-C8 haloalkyl or C2-C8 alkoxyalkyl;
    Rb10 is halogen, C1-C2 alkyl or C1-C2 haloalkyl;
    Rb11 is halogen, C1-C2 alkyl or C1-C2 haloalkyl;
    Rb12 is C1-C2 alkyl;
    Rb13 is H, halogen or C1-C2 alkyl;
    Rb14 is C1-C2 alkyl or C1-C2 haloalkyl;
    Rb15 is H, C1-C2 alkyl or C1-C2 haloalkyl;
    • W is CH or N; Y is CH or N; and Z is CH or N.
  • Component (b10a) relates to isofetamid (IKF-5411), which is N-[1,1-dimethyl-2-[2-methyl-4-(1-methylethoxy)phenyl]-2-oxoethyl]-3-methyl-2-thiophenecarboxamide (Registry Number 875915-78-9), i.e. the compound of Formula B10a
  • Figure US20150018374A1-20150115-C00055
  • This compound as well as the compounds of Component (b10) can be prepared by methods described in PCT Patent Publications WO 2006/016708 and WO 2007/069777.
  • Component (b10b) relates to tolprocarb (MTF-0301), which is 2,2,2-trifluoroethyl N-[(1S)-2-methyl-1-[[(4-methylbenzoyl)amino]methyl]propyl]carbamate (Registry Number 911499-62-2), i.e. the compound of Formula B10b
  • Figure US20150018374A1-20150115-C00056
  • This compound can be prepared by methods described in US Patent Publication US 2007/0049635 A1.
  • Component (b11) relates to the compound of Formula B11
  • Figure US20150018374A1-20150115-C00057
  • which is (αR)-2-[(2,5-dimethylphenoxy)methyl]-α-methoxy-N-methylbenzeneacetamide (Registry Number 394657-24-0). The compound of Formula B11 can be prepared by methods described in PCT Patent Publication WO 95/27693.
  • Component (b12) relates to the compound of Formula B12
  • Figure US20150018374A1-20150115-C00058
  • which is 2,6-dimethyl-1H,5H-[1,4]dithiino[2,3-c:5,6-c′]dipyrrole-1,3,5,7(2H,6H)-tetrone (Registry Number 16114-35-5). The compound of Formula B12 can be prepared by methods described in U.S. Pat. No. 3,364,229.
  • Component (b13) relates to the compound of Formula B13
  • Figure US20150018374A1-20150115-C00059
  • which is N-cyclopropyl-3-(difluoromethyl)-5-fluoro-1-methyl-N-[[2-(1-methylethyl)phenyl]-methyl]-1H-pyrazole-4-carboxamide (Registry Number 1255733-83-5). The compound of Formula B13 can be prepared by methods described in PCT Patent Publication WO 2010/130767.
  • Compositions comprising a combination of (a) at least one compound selected from the compounds of Formula 1, including N-oxides and salts thereof, together with (b) at least one fungicidal component selected from Formulae B1 through B13, including salts thereof, described above typically will provide improved control (i.e. prevention and/or cure) of plant disease from synergic contributions of components (a) and (b). The improved plant disease control may be manifest by a broader spectrum or longer duration of plant disease control, or retardation of resistance development. The contributions of components (a) and (b) may be complementarily additive or even greater than additive through synergistic interaction.
  • This invention also relates to a fungicidal composition comprising: (a) at least one compound selected from the compounds of Formula 1, (b) at least one fungicidal compound selected from Formulae B1 through B13 described above, and (c) further comprising at least one additional compound or agent that is biologically active. Thus compositions of component (a) with component (b) can be further mixed with (c) one or more other biologically active compounds or agents including insecticides, nematocides, bactericides, acaricides, herbicides, herbicide safeners, growth regulators such as insect molting inhibitors and rooting stimulants, chemosterilants, semiochemicals, repellents, attractants, pheromones, feeding stimulants, plant nutrients, other biologically active compounds or entomopathogenic bacteria, virus or fungi to form a multi-component pesticide giving an even broader spectrum of agricultural protection. General references for these agricultural protectants include The Pesticide Manual, 13th Edition, C. D. S. Tomlin, Ed., British Crop Protection Council, Farnham, Surrey, U.K., 2003 and The BioPesticide Manual, 2nd Edition, L. G. Copping, Ed., British Crop Protection Council, Farnham, Surrey, U.K., 2001.
  • A more particular aspect relates to said fungicidal composition wherein component (c) comprises at least one additional compound that is a fungicide (i.e. an additional fungicidal compound). In the present composition, additional fungicidal compounds in component (c) are typically selected from the group consisting of (c1) methyl benzimidazole carbamate (MBC) fungicides; (c2) dicarboximide fungicides; (c3) demethylation inhibitor (DMI) fungicides; (c4) phenylamide fungicides; (c5) amine/morpholine fungicides; (c6) phospholipid biosynthesis inhibitor fungicides; (c7) carboxamide fungicides; (c8) hydroxy(2-amino-)pyrimidine fungicides; (c9) anilinopyrimidine fungicides; (c10) N-phenyl carbamate fungicides; (c11) quinone outside inhibitor (QoI) fungicides; (c12) phenylpyrrole fungicides; (c13) quinoline fungicides; (c14) lipid peroxidation inhibitor fungicides; (c15) melanin biosynthesis inhibitors-reductase (MBI-R) fungicides; (c16) melanin biosynthesis inhibitors-dehydratase (MBI-D) fungicides; (c17) hydroxyanilide fungicides; (c18) squalene-epoxidase inhibitor fungicides; (c19) polyoxin fungicides; (c20) phenylurea fungicides; (c21) quinone inside inhibitor (QiI) fungicides; (c22) benzamide fungicides; (c23) enopyranuronic acid antibiotic fungicides; (c24) hexopyranosyl antibiotic fungicides; (c25) glucopyranosyl antibiotic: protein synthesis fungicides; (c26) glucopyranosyl antibiotic: trehalase and inositol biosynthesis fungicides; (c27) cyanoacetamideoxime fungicides; (c28) carbamate fungicides; (c29) oxidative phosphorylation uncoupling fungicides; (c30) organo tin fungicides; (c31) carboxylic acid fungicides; (c32) heteroaromatic fungicides; (c33) phosphonate fungicides; (c34) phthalamic acid fungicides; (c35) benzotriazine fungicides; (c36) benzene-sulfonamide fungicides; (c37) pyridazinone fungicides; (c38) thiophene-carboxamide fungicides; (c39) pyrimidinamide fungicides; (c40) carboxylic acid amide (CAA) fungicides; (c41) tetracycline antibiotic fungicides; (c42) thiocarbamate fungicides; (c43) benzamide fungicides; (c44) host plant defense induction fungicides; (c45) multi-site contact activity fungicides; (c46) fungicides other than fungicides of component (a) and components (c1) through (c45); and salts of compounds of (c1) through (c46).
  • Of note are fungicide composition embodiments wherein component (c) comprises at least one fungicidal compound from each of two different groups selected from (c1) through (c46).
  • “Methyl benzimidazole carbamate (MBC) fungicides (c1)” (FRAC (Fungicide Resistance Action Committee) code 1) inhibit mitosis by binding to 3-tubulin during microtubule assembly. Inhibition of microtubule assembly can disrupt cell division, transport within the cell and cell structure. Methyl benzimidazole carbamate fungicides include benzimidazole and thiophanate fungicides. The benzimidazoles include benomyl, carbendazim, fuberidazole and thiabendazole. The thiophanates include thiophanate and thiophanate-methyl.
  • “Dicarboximide fungicides (c2)” (FRAC code 2) are proposed to inhibit a lipid peroxidation in fungi through interference with NADH cytochrome c reductase. Examples include chlozolinate, iprodione, procymidone and vinclozolin.
  • “Demethylation inhibitor (DMI) fungicides (c3)” (FRAC code 3) inhibit C14-demethylase which plays a role in sterol production. Sterols, such as ergosterol, are needed for membrane structure and function, making them essential for the development of functional cell walls. Therefore, exposure to these fungicides result in abnormal growth and eventually death of sensitive fungi. DMI fungicides are divided between several chemical classes: azoles (including triazoles and imidazoles), pyrimidines, piperazines and pyridines. The triazoles include azaconazole, bitertanol, bromuconazole, cyproconazole, difenoconazole, diniconazole (including diniconazole-M), epoxiconazole, etaconazole, fenbuconazole, fluquinconazole, flusilazole, flutriafol, hexaconazole, imibenconazole, ipconazole, metconazole, myclobutanil, penconazole, propiconazole, prothioconazole, quinconazole, simeconazole, tebuconazole, tetraconazole, triadimefon, triadimenol, triticonazole and uniconazole. The imidazoles include clotrimazole, econazole, imazalil, isoconazole, miconazole, oxpoconazole, prochloraz, pefurazoate and triflumizole. The pyrimidines include fenarimol, nuarimol and triarimol. The piperazines include triforine. The pyridines include buthiobate and pyrifenox. Biochemical investigations have shown that all of the above mentioned fungicides are DMI fungicides as described by K. H. Kuck et al. in Modern Selective Fungicides—Properties, Applications and Mechanisms of Action, H. Lyr (Ed.), Gustav Fischer Verlag: New York, 1995, 205-258.
  • “Phenylamide fungicides (c4)” (FRAC code 4) are specific inhibitors of RNA polymerase in Oomycete fungi. Sensitive fungi exposed to these fungicides show a reduced capacity to incorporate uridine into rRNA. Growth and development in sensitive fungi is prevented by exposure to this class of fungicide. Phenylamide fungicides include acylalanine, oxazolidinone and butyrolactone fungicides. The acylalanines include benalaxyl, benalaxyl-M, furalaxyl, metalaxyl, metalaxyl-M (also known as mefenoxam). The oxazolidinones include oxadixyl. The butyrolactones include ofurace.
  • “Amine/morpholine fungicides (c5)” (FRAC code 5) inhibit two target sites within the sterol biosynthetic pathway, Δ8→Δ7 isomerase and Δ14 reductase. Sterols, such as ergosterol, are needed for membrane structure and function, making them essential for the development of functional cell walls. Therefore, exposure to these fungicides results in abnormal growth and eventually death of sensitive fungi. Amine/morpholine fungicides (also known as non-DMI sterol biosynthesis inhibitors) include morpholine, piperidine and spiroketal-amine fungicides. The morpholines include aldimorph, dodemorph, fenpropimorph, tridemorph and trimorphamide. The piperidines include fenpropidin and piperalin. The spiroketal-amines include spiroxamine.
  • “Phospholipid biosynthesis inhibitor fungicides (c6)” (FRAC code 6) inhibit growth of fungi by affecting phospholipid biosynthesis. Phospholipid biosynthesis fungicides include phosphorothiolate and dithiolane fungicides. The phosphorothiolates include edifenphos, iprobenfos and pyrazophos. The dithiolanes include isoprothiolane.
  • “Carboxamide fungicides (c7)” (FRAC code 7) inhibit Complex II (succinate dehydrogenase) fungal respiration by disrupting a key enzyme in the Krebs Cycle (TCA cycle) named succinate dehydrogenase Inhibiting respiration prevents the fungus from making ATP, and thus inhibits growth and reproduction. Carboxamide fungicides include benzamide, furan carboxamide, oxathiin carboxamide, thiazole carboxamide, pyrazole carboxamide and pyridine carboxamide. The benzamides include benodanil, flutolanil and mepronil. The furan carboxamides include fenfuram. The oxathiin carboxamides include carboxin and oxycarboxin. The thiazole carboxamides include thifluzamide. The pyrazole carboxamides include bixafen, furametpyr, isopyrazam, fluxapyroxad, penthiopyrad, sedaxane (N-[2-(1S,2R)-[1,1′-bicyclopropyl]-2-ylphenyl]-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxamide) and penflufen (N-[2-(1,3-dimethylbutyl)phenyl]-5-fluoro-1,3-dimethyl-1H-pyrazole-4-carboxamide) (PCT Patent Publication WO 2003/010149). The pyridine carboxamides include boscalid.
  • “Hydroxy(2-amino-)pyrimidine fungicides (c8)” (FRAC code 8) inhibit nucleic acid synthesis by interfering with adenosine deaminase. Examples include bupirimate, dimethirimol and ethirimol.
  • “Anilinopyrimidine fungicides (c9)” (FRAC code 9) are proposed to inhibit biosynthesis of the amino acid methionine and to disrupt the secretion of hydrolytic enzymes that lyse plant cells during infection. Examples include cyprodinil, mepanipyrim and pyrimethanil.
  • “N-Phenyl carbamate fungicides (c10)” (FRAC code 10) inhibit mitosis by binding to β-tubulin and disrupting microtubule assembly. Inhibition of microtubule assembly can disrupt cell division, transport within the cell and cell structure. Examples include diethofencarb.
  • “Quinone outside inhibitor (QoI) fungicides (c11)” (FRAC code 11) inhibit Complex III mitochondrial respiration in fungi by affecting ubiquinol oxidase. Oxidation of ubiquinol is blocked at the “quinone outside” (Qo) site of the cytochrome bc1 complex, which is located in the inner mitochondrial membrane of fungi Inhibiting mitochondrial respiration prevents normal fungal growth and development. Quinone outside inhibitor fungicides include methoxyacrylate, methoxycarbamate, oximinoacetate, oximinoacetamide and dihydrodioxazine fungicides (collectively also known as strobilurin fungicides), and oxazolidinedione, imidazolinone and benzylcarbamate fungicides. The methoxyacrylates include azoxystrobin, enestroburin (SYP-Z071) and picoxystrobin. The methoxycarbamates include pyraclostrobin and pyrametostrobin. The oximinoacetates include kresoxim-methyl, pyraoxystrobin and trifloxystrobin. The oximinoacetamides include dimoxystrobin, metominostrobin, orysastrobin and α-(methoxyimino)-N-methyl-2-[[[1-[3-(trifluoro-methyl)phenyl]ethoxy]imino]methyl]benzeneacetamide. The dihydrodioxazines include fluoxastrobin. The oxazolidinediones include famoxadone. The imidazolinones include fenamidone. The benzylcarbamates include pyribencarb.
  • “Phenylpyrrole fungicides (c12)” (FRAC code 12) inhibit a MAP protein kinase associated with osmotic signal transduction in fungi. Fenpiclonil and fludioxonil are examples of this fungicide class.
  • “Quinoline fungicides (c13)” (FRAC code 13) are proposed to inhibit signal transduction by affecting G-proteins in early cell signaling. They have been shown to interfere with germination and/or appressorium formation in fungi that cause powdery mildew diseases. Quinoxyfen is an example of this class of fungicide.
  • “Lipid peroxidation inhibitor fungicides (c14)” (FRAC code 14) are proposed to inhibit lipid peroxidation which affects membrane synthesis in fungi. Members of this class, such as etridiazole, may also affect other biological processes such as respiration and melanin biosynthesis. Lipid peroxidation fungicides include aromatic carbon and 1,2,4-thiadiazole fungicides. The aromatic carbons include biphenyl, chloroneb, dicloran, quintozene, tecnazene and tolclofos-methyl. The 1,2,4-thiadiazoles include etridiazole.
  • “Melanin biosynthesis inhibitors-reductase (MBI-R) fungicides (c15)” (FRAC code 16.1) inhibit the naphthal reduction step in melanin biosynthesis. Melanin is required for host plant infection by some fungi. Melanin biosynthesis inhibitors-reductase fungicides include isobenzofuranone, pyrroloquinolinone and triazolobenzothiazole fungicides. The isobenzofuranones include fthalide. The pyrroloquinolinones include pyroquilon. The triazolobenzothiazoles include tricyclazole.
  • “Melanin biosynthesis inhibitors-dehydratase (MBI-D) fungicides (c16)” (FRAC code 16.2) inhibit scytalone dehydratase in melanin biosynthesis. Melanin in required for host plant infection by some fungi. Melanin biosynthesis inhibitors-dehydratase fungicides include cyclopropanecarboxamide, carboxamide and propionamide fungicides. The cyclopropanecarboxamides include carpropamid. The carboxamides include diclocymet. The propionamides include fenoxanil.
  • “Hydroxyanilide fungicides (c17)” (FRAC code 17) inhibit C4-demethylase which plays a role in sterol production. Examples include fenhexamid.
  • “Squalene-epoxidase inhibitor fungicides (c18)” (FRAC code 18) inhibit squalene-epoxidase in ergosterol biosynthesis pathway. Sterols such as ergosterol are needed for membrane structure and function, making them essential for the development of functional cell walls. Therefore exposure to these fungicides result in abnormal growth and eventually death of sensitive fungi. Squalene-epoxidase inhibitor fungicides include thiocarbamate and allylamine fungicides. The thiocarbamates include pyributicarb. The allylamines include naftifine and terbinafine.
  • “Polyoxin fungicides (c19)” (FRAC code 19) inhibit chitin synthase. Examples include polyoxin.
  • “Phenylurea fungicides (c20)” (FRAC code 20) are proposed to affect cell division. Examples include pencycuron.
  • “Quinone inside inhibitor (QiI) fungicides (c21)” (FRAC code 21) inhibit Complex III mitochondrial respiration in fungi by affecting ubiquinol reductase. Reduction of ubiquinol is blocked at the “quinone inside” (Qi) site of the cytochrome bc1 complex, which is located in the inner mitochondrial membrane of fungi. Inhibiting mitochondrial respiration prevents normal fungal growth and development. Quinone inside inhibitor fungicides include cyanoimidazole and sulfamoyltriazole fungicides. The cyanoimidazoles include cyazofamid. The sulfamoyltriazoles include amisulbrom.
  • “Benzamide fungicides (c22)” (FRAC code 22) inhibit mitosis by binding to 3-tubulin and disrupting microtubule assembly Inhibition of microtubule assembly can disrupt cell division, transport within the cell and cell structure. Examples include zoxamide.
  • “Enopyranuronic acid antibiotic fungicides (c23)” (FRAC code 23) inhibit growth of fungi by affecting protein biosynthesis. Examples include blasticidin-S.
  • “Hexopyranosyl antibiotic fungicides (c24)” (FRAC code 24) inhibit growth of fungi by affecting protein biosynthesis. Examples include kasugamycin.
  • “Glucopyranosyl antibiotic: protein synthesis fungicides (c25)” (FRAC code 25) inhibit growth of fungi by affecting protein biosynthesis. Examples include streptomycin.
  • “Glucopyranosyl antibiotic: trehalase and inositol biosynthesis fungicides (c26)” (FRAC code 26) inhibit trehalase in inositol biosynthesis pathway. Examples include validamycin.
  • “Cyanoacetamideoxime fungicides (c27)” (FRAC code 27) include cymoxanil.
  • “Carbamate fungicides (c28)” (FRAC code 28) are considered multi-site inhibitors of fungal growth. They are proposed to interfere with the synthesis of fatty acids in cell membranes, which then disrupts cell membrane permeability. Propamacarb, iodocarb, and prothiocarb are examples of this fungicide class.
  • “Oxidative phosphorylation uncoupling fungicides (c29)” (FRAC code 29) inhibit fungal respiration by uncoupling oxidative phosphorylation Inhibiting respiration prevents normal fungal growth and development. This class includes 2,6-dinitroanilines such as fluazinam, pyrimidonehydrazones such as ferimzone and dinitrophenyl crotonates such as dinocap, meptyldinocap and binapacryl.
  • “Organo tin fungicides (c30)” (FRAC code 30) inhibit adenosine triphosphate (ATP) synthase in oxidative phosphorylation pathway. Examples include fentin acetate, fentin chloride and fentin hydroxide.
  • “Carboxylic acid fungicides (c31)” (FRAC code 31) inhibit growth of fungi by affecting deoxyribonucleic acid (DNA) topoisomerase type II (gyrase). Examples include oxolinic acid.
  • “Heteroaromatic fungicides (c32)” (FRAC code 32) are proposed to affect DNA/ribonucleic acid (RNA) synthesis. Heteroaromatic fungicides include isoxazole and isothiazolone fungicides. The isoxazoles include hymexazole and the isothiazolones include octhilinone.
  • “Phosphonate fungicides (c33)” (FRAC code 33) include phosphorous acid and its various salts, including fosetyl-aluminum.
  • “Phthalamic acid fungicides (c34)” (FRAC code 34) include teclofthalam.
  • “Benzotriazine fungicides (c35)” (FRAC code 35) include triazoxide.
  • “Benzene-sulfonamide fungicides (c36)” (FRAC code 36) include flusulfamide.
  • “Pyridazinone fungicides (c37)” (FRAC code 37) include diclomezine.
  • “Thiophene-carboxamide fungicides (c38)” (FRAC code 38) are proposed to affect ATP production. Examples include silthiofam.
  • “Pyrimidinamide fungicides (c39)” (FRAC code 39) inhibit growth of fungi by affecting phospholipid biosynthesis and include diflumetorim.
  • “Carboxylic acid amide (CAA) fungicides (c40)” (FRAC code 40) are proposed to inhibit phospholipid biosynthesis and cell wall deposition. Inhibition of these processes prevents growth and leads to death of the target fungus. Carboxylic acid amide fungicides include cinnamic acid amide, valinamide carbamate and mandelic acid amide fungicides. The cinnamic acid amides include dimethomorph and flumorph. The valinamide carbamates include benthiavalicarb, benthiavalicarb-isopropyl, iprovalicarb and valifenalate (valiphenal). The mandelic acid amides include mandipropamid, N-[2-[4-[[3-(4-chlorophenyl)-2-propyn-1-yl]oxy]-3-methoxyphenyl]ethyl]-3-methyl-2-[(methylsulfonyl)-amino]butanamide and N-[2-[4-[[3-(4-chlorophenyl)-2-propyn-1-yl]oxy]-3-methoxyphenyl]-ethyl]-3-methyl-2-[(ethylsulfonyl)amino]butanamide.
  • “Tetracycline antibiotic fungicides (c41)” (FRAC code 41) inhibit growth of fungi by affecting complex 1 nicotinamide adenine dinucleotide (NADH) oxidoreductase. Examples include oxytetracycline.
  • “Thiocarbamate fungicides (c42)” (FRAC code 42) include methasulfocarb.
  • “Benzamide fungicides (c43)” (FRAC code 43) inhibit growth of fungi by delocalization of spectrin-like proteins. Examples include acylpicolide fungicides such as fluopicolide and fluopyram.
  • “Host plant defense induction fungicides (c44)” (FRAC code P) induce host plant defense mechanisms. Host plant defense induction fungicides include benzo-thiadiazole, benzisothiazole and thiadiazole-carboxamide fungicides. The benzo-thiadiazoles include acibenzolar-S-methyl. The benzisothiazoles include probenazole. The thiadiazole-carboxamides include tiadinil and isotianil.
  • “Multi-site contact fungicides (c45)” inhibit fungal growth through multiple sites of action and have contact/preventive activity. This class of fungicides includes: “copper fungicides (c45.1) (FRAC code M1)”, “sulfur fungicides (c45.2) (FRAC code M2)”, “dithiocarbamate fungicides (c45.3) (FRAC code M3)”, “phthalimide fungicides (c45.4) (FRAC code M4)”, “chloronitrile fungicides (c45.5) (FRAC code M5)”, “sulfamide fungicides (c45.6) (FRAC code M6)”, “guanidine fungicides (c45.7) (FRAC code M7)” “triazine fungicides (c45.8) (FRAC code M8)” and “quinone fungicides (c45.9) (FRAC code M9)”. “Copper fungicides” are inorganic compounds containing copper, typically in the copper(II) oxidation state; examples include copper oxychloride, copper sulfate and copper hydroxide, including compositions such as Bordeaux mixture (tribasic copper sulfate). “Sulfur fungicides” are inorganic chemicals containing rings or chains of sulfur atoms; examples include elemental sulfur. “Dithiocarbamate fungicides” contain a dithiocarbamate molecular moiety; examples include mancozeb, metiram, propineb, ferbam, maneb, thiram, zineb and ziram. “Phthalimide fungicides” contain a phthalimide molecular moiety; examples include folpet, captan and captafol. “Chloronitrile fungicides” contain an aromatic ring substituted with chloro and cyano; examples include chlorothalonil. “Sulfamide fungicides” include dichlofluanid and tolylfluanid. “Guanidine fungicides” include dodine, guazatine and iminoctadine. “Triazine fungicides” include anilazine. “Quinone fungicides” include dithianon.
  • “Fungicides other than fungicides of component (a) and components (c1) through (c45); (c46)” include certain fungicides whose mode of action may be unknown. These include: (c46.1) “thiazole carboxamide fungicides” (FRAC code U5), (c46.2) “phenyl-acetamide fungicides” (FRAC code U6), (c46.3) “quinazolinone fungicides” (FRAC code U7), (c46.4) “benzophenone fungicides” (FRAC code U8) and (c46.5) “triazolopyrimidylamine fungicides” (FRAC code 45). The thiazole carboxamides include ethaboxam. The phenyl-acetamides include cyflufenamid and N-[[(cyclopropyl-methoxy)amino][6-(difluoromethoxy)-2,3-difluorophenyl]-methylene]benzeneacetamide. The quinazolinones include proquinazid and 2-butoxy-6-iodo-3-propyl-4H-1-benzopyran-4-one. The benzophenones include metrafenone and pyriofenone. The triazolopyrimidylamines include ametoctradin and are believed to inhibit Complex III mitochondrial respiration by binding to an unelucidated site on ubiquinone-cytochrome bc1 reductase. The (c46) class also includes bethoxazin, neo-asozin (ferric methanearsonate), fenpyrazamine, pyrrolnitrin, quinomethionate, tebufloquin, 2-[[2-fluoro-5-(trifluoromethyl)phenyl]thio]-2-[3-(2-methoxyphenyl)-2-thiazolidinylidene]acetonitrile, 3-[5-(4-chlorophenyl)-2,3-dimethyl-3-isoxazolidinyl]pyridine, 4-fluorophenyl N-[1-[[[1-(4-cyanophenyl)ethyl]sulfonyl]methyl]propyl]carbamate, 5-chloro-6-(2,4,6-trifluorophenyl)-7-(4-methylpiperidin-1-yl) [1,2,4]triazolo[1,5-a]pyrimidine, N-(4-chloro-2-nitrophenyl)-N-ethyl-4-methylbenzenesulfonamide, N′-[4-[4-chloro-3-(trifluoromethyl)phenoxy]-2,5-dimethylphenyl]-N-ethyl-N-methylmethanimidamide and 1-[(2-propenylthio)carbonyl]-2-(1-methylethyl)-4-(2-methylphenyl)-5-amino-1H-pyrazol-3-one.
  • “Fungicides other than fungicides of component (a) and components (c1) through (c45); (c46)” also include (c46.5) 6-quinolinyloxyacetamide compounds of Formula C1 and salts thereof
  • Figure US20150018374A1-20150115-C00060
  • wherein
      • Rc1 is halogen, C1-C4 alkoxy or C1-C4 alkynyl;
      • Rc2 is H, halogen or C1-C4 alkyl;
      • Rc3 is C1-C12 alkyl, C1-C12 haloalkyl, C1-C12 alkoxy, C2-C12 alkoxyalkyl, C2-C12 alkenyl, C2-C12 alkynyl, C4-C12 alkoxyalkenyl, C4-C12 alkoxyalkynyl, C1-C12 alkylthio or C2-C12 alkylthioalkyl;
      • Rc4 is methyl or —Ya1—Rc5;
      • Rc5 is C1-C2 alkyl; and
      • Yc1 is CH2, O or S.
        Compounds of Formula C1, their use as fungicides and methods of preparation are generally known; see, for example, PCT Patent Publications WO 2004/047538, WO 2004/108663, WO 2006/058699, WO 2006/058700, WO 2008/110355, WO 2009/030469, WO 2009/049716 and WO 2009/087098. Examples of compounds of Formula C1 include: 2-[(3-bromo-6-quinolinyl)oxy]-N-(1,1-dimethyl-2-butyn-1-yl)-2-(methylthio)acetamide, 2-[(3-ethynyl-6-quinolinyl)oxy]-N-[1-(hydroxymethyl)-1-methyl-2-propyn-1-yl]-2-(methyl-thio)acetamide, N-(1,1-dimethyl-2-butyn-1-yl)-2-[(3-ethynyl-6-quinolinyl)oxy]-2-(methyl-thio)acetamide, 2-[(3-bromo-8-methyl-6-quinolinyl)oxy]-N-(1,1-dimethyl-2-propyn-1-yl)-2-(methylthio)acetamide and 2-[(3-bromo-6-quinolinyl)oxy]-N-(1,1-dimethylethyl)-butanamide.
  • “Fungicides other than fungicides of component (a) and components (c1) through (c45); (c46)” also include (c46.6) N′-[4-[[3-[(4-chlorophenyl)methyl]-1,2,4-thiadiazol-5-yl]oxy]-2,5-dimethylphenyl]-N-ethyl-N-methylmethanimidamide, which is believed to inhibit C24-methyl transferase involved in biosynthesis of sterols.
  • Examples of component (c) fungicidal compounds include those listed in Embodiment 31, more particularly Embodiment 32, and even more particularly Embodiment 33.
  • Compositions comprising a combination of (a) at least one compound selected from the compounds of Formula 1, including N-oxides and salts thereof, (b) at least one fungicidal component selected from Formulae B1 through B13, including salts thereof and (c) at least one additional fungicidal compound (e.g., (c1) through (c46) of Embodiment 30, including the corresponding fungicidal compounds described above) can provide improved control (i.e. prevention and/or cure) of plant disease from synergic contributions of components (a), (b) and (c). The improved plant disease control may be manifest by a broader spectrum or longer duration of plant disease control, or retardation of resistance development. The contributions of components (a), (b) and (c) may be complementarily additive or even greater than additive through synergistic interaction. Addition of component (c) may provide stronger synergy than resulting from combination of components (a) and (b).
  • In a fungicidal composition comprising (a) at least one compound selected from the compounds of Formula 1, including N-oxides and salts thereof, (b) at least one fungicidal compound selected from Formulae B1 through B13 including salts thereof, described above, and (c) further comprising at least one additional compound or agent that is biologically active, besides the fungicidal compounds (c1) through (c46) described above, component (c) can also be selected from compounds or agents having biological activity that is other than fungicidal. Examples of such biologically active compounds or agents with which compositions of component (a) with component (b), can be mixed (e.g., in an agricultural formulation) are: insecticides such as abamectin, acephate, acetamiprid, acetoprole, acrinathrin, aldicarb, amidoflumet, amitraz, avermectin, azadirachtin, azinphos-methyl, bifenthrin, bifenazate, bistrifluron, buprofezin, carbofuran, cartap, chinomethionat, chlorfenapyr, chlorfluazuron, chlorantraniliprole, chlorpyrifos, chlorpyrifos-methyl, chlorobenzilate, chromafenozide, clothianidin, cyantraniliprole, cyflumetofen, cyfluthrin, beta-cyfluthrin, cyhalothrin, gamma-cyhalothrin, lambda-cyhalothrin, cyhexatin, cypermethrin, cyromazine, deltamethrin, diafenthiuron, diazinon, dicofol, dieldrin, dienochlor, diflubenzuron, dimefluthrin, dimethoate, dinotefuran, diofenolan, emamectin, endosulfan, esfenvalerate, ethiprole, etoxazole, fenamiphos, fenazaquin, fenbutatin oxide, fenothiocarb, fenoxycarb, fenpropathrin, fenpyroximate, fenvalerate, fipronil, flonicamid, flubendiamide, flucythrinate, tau-fluvalinate, flufenerim, flufenoxuron, fonophos, halofenozide, hexaflumuron, hexythiazox, hydramethylnon, imicyafos, imidacloprid, indoxacarb, isofenphos, lufenuron, malathion, meperfluthrin, metaflumizone, metaldehyde, methamidophos, methidathion, methomyl, methoprene, methoxychlor, methoxyfenozide, metofluthrin, milbemycin oxime, monocrotophos, nicotine, nitenpyram, nithiazine, novaluron, noviflumuron, oxamyl, parathion, parathion-methyl, permethrin, phorate, phosalone, phosmet, phosphamidon, pirimicarb, profenofos, profluthrin, propargite, prothiocarb, protrifenbute, pymetrozine, pyrafluprole, pyrethrin, pyridaben, pyridalyl, pyrifluquinazon, pyriprole, pyriproxyfen, rotenone, ryanodine, spinetoram, spinosad, spiridiclofen, spiromesifen, spirotetramat, sulfoxaflor, sulprofos, tebufenozide, tebufenpyrad, teflubenzuron, tefluthrin, terbufos, tetrachlorvinphos, tetramethylfluthrin, thiacloprid, thiamethoxam, thiodicarb, thiosultap-sodium, tolfenpyrad, tralomethrin, triazamate, trichlorfon, triflumuron; nematocides such as aldicarb, imicyafos, oxamyl and fenamiphos; bactericides such as streptomycin; acaricides such as amitraz, chinomethionat, chlorobenzilate, cyenopyrafen, cyhexatin, dicofol, dienochlor, etoxazole, fenazaquin, fenbutatin oxide, fenpropathrin, fenpyroximate, hexythiazox, propargite, pyridaben and tebufenpyrad; and biological agents including entomopathogenic bacteria, such as Bacillus thuringiensis subsp. aizawai, Bacillus thuringiensis subsp. kurstaki, and the encapsulated delta-endotoxins of Bacillus thuringiensis (e.g., Cellcap, MPV, MPVII); entomopathogenic fungi, such as green muscardine fungus; and entomopathogenic virus including baculovirus, nucleopolyhedro virus (NPV) such as HzNPV, AfNPV; and granulosis virus (GV) such as CpGV.
  • Of note is a composition of the present invention which comprises, in addition to a components (a) and (b), at least one invertebrate pest control compound or agent selected from the group consisting of abamectin, acephate, acetamiprid, acetoprole, acrinathrin, aldicarb, amidoflumet, amitraz, avermectin, azadirachtin, azinphos-methyl, bifenthrin, bifenazate, bistrifluron, buprofezin, carbofuran, cartap, chinomethionat, chlorfenapyr, chlorfluazuron, chlorantraniliprole, chlorpyrifos, chlorpyrifos-methyl, chlorobenzilate, chromafenozide, clothianidin, cyantraniliprole, cyflumetofen, cyfluthrin, beta-cyfluthrin, cyhalothrin, gamma-cyhalothrin, lambda-cyhalothrin, cyhexatin, cypermethrin, cyromazine, deltamethrin, diafenthiuron, diazinon, dicofol, dieldrin, dienochlor, diflubenzuron, dimefluthrin, dimethoate, dinotefuran, diofenolan, emamectin, endosulfan, esfenvalerate, ethiprole, etoxazole, fenamiphos, fenazaquin, fenbutatin oxide, fenothiocarb, fenoxycarb, fenpropathrin, fenpyroximate, fenvalerate, fipronil, flonicamid, flubendiamide, flucythrinate, tau-fluvalinate, flufenerim, flufenoxuron, fonophos, halofenozide, hexaflumuron, hexythiazox, hydramethylnon, imicyafos, imidacloprid, indoxacarb, isofenphos, lufenuron, malathion, meperfluthrin, metaflumizone, metaldehyde, methamidophos, methidathion, methomyl, methoprene, methoxychlor, methoxyfenozide, metofluthrin, milbemycin oxime, monocrotophos, nicotine, nitenpyram, nithiazine, novaluron, noviflumuron, oxamyl, parathion, parathion-methyl, permethrin, phorate, phosalone, phosmet, phosphamidon, pirimicarb, profenofos, profluthrin, propargite, protrifenbute, pymetrozine, pyrafluprole, pyrethrin, pyridaben, pyridalyl, pyrifluquinazon, pyriprole, pyriproxyfen, rotenone, ryanodine, spinetoram, spinosad, spiridiclofen, spiromesifen, spirotetramat, sulfoxaflor, sulprofos, tebufenozide, tebufenpyrad, teflubenzuron, tefluthrin, terbufos, tetrachlorvinphos, tetramethylfluthrin, thiacloprid, thiamethoxam, thiodicarb, thiosultap-sodium, tolfenpyrad, tralomethrin, triazamate, trichlorfon, triflumuron, Bacillus thuringiensis subsp. aizawai, Bacillus thuringiensis subsp. kurstaki, nucleopolyhedro viruses, encapsulated delta-endotoxins of Bacillus thuringiensis, baculoviruses, entomopathogenic bacteria, entomopathogenic viruses and entomopathogenic fungi.
  • In certain instances, combinations of a mixture of components (a) and (b) fungicidal compounds with invertebrate pest control compounds or agents (i.e. as component (c) biologically active ingredients) can result in a greater-than-additive (i.e. synergistic) effect. Reducing the quantity of active ingredients released in the environment while ensuring effective pest control is always desirable. When synergism of invertebrate pest control active ingredients occurs at application rates giving agronomically satisfactory levels of invertebrate pest control, such combinations can be advantageous for reducing crop production cost and decreasing environmental load. Synergism can also result in increased plant disease control or protection.
  • In the fungicidal compositions of the present invention, component (a) (i.e. at least one compound selected from compounds of Formula 1, N-oxides, and salts thereof) and component (b) are present in fungicidally effective amounts. The weight ratio of component (a) to component (b) (i.e. one or more additional fungicidal compounds) is generally between about 1:3000 to about 3000:1, more typically between about 1:500 and about 500:1. Of note are compositions where in the weight ratio of component (a) to component (b) is from about 125:1 to about 1:125. With many fungicidal compounds of component (b), these compositions are particularly effective for controlling plant diseases caused by fungal plant pathogens. Of particular note are compositions wherein the weight ratio of component (a) to component (b) is from about 25:1 to about 1:25, or from about 5:1 to about 1:5. One skilled in the art can easily determine through simple experimentation the weight ratios and application rates of fungicidal compounds necessary for the desired spectrum of fungicidal protection and control.
  • Table A1 lists specific combinations of a Component (b) compound with Compound 1 as Component (a) illustrative of the mixtures, compositions and methods of the present invention. (Compound numbers refer to compounds in Index Table A.) The second column of Table A1 lists the specific Component (b) compound (e.g., “1-[4-[4-[5-(2,6-difluorophenyl)-4,5-dihydro-3-isoxazolyl]-2-thiazolyl]-1-piperidinyl]-2-[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]ethanone (b1a)” in the first line). The third, fourth and fifth columns of Table A1 lists ranges of weight ratios for rates at which the Component (a) compound is typically applied to a field-grown crop relative to Component (b). Thus, for example, the first line of Table A1 specifically discloses the combination of Compound 1 with Component (b1a) is typically applied in a weight ratio of Compound 1 to Component (b1a) of between 400:1 and 1:1. The remaining lines of Table A1 are to be construed similarly.
  • TABLE A1
    More
    Typical Typical
    Component Weight Weight Most Typical
    (a) Component (b) Ratio Ratio Weight Ratio
    Compound 1 1-[4-[4-[5-(2,6-difluorophenyl)-4,5-dihydro- 400:1 to 1:1  100:1 to 4:1  50:1 to 8:1 
    3-isoxazolyl]-2-thiazolyl]-1-piperidinyl]-2-[5-
    methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]-
    ethanone (b1a)
    Compound 1 1-[4-[4-[5R-(2,6-difluorophenyl)-4,5-dihydro- 800:1 to 2:1  200:1 to 8:1  100:1 to 16:1 
    3-isoxazolyl]-2-thiazolyl]-1-piperidinyl]-2-[5-
    methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]-
    ethanone (b1aa)
    Compound 1 1-[4-[4-[5-[(2,6-difluorophenoxy)methyl]-4,5- 400:1 to 1:1  100:1 to 4:1  50:1 to 8:1 
    dihydro-3-isoxazolyl]-2-thiazolyl]-1-
    piperdinyl-2-[5-methyl-3-(trifluoromethyl)-
    1H-pyrazol-1-yl]ethanone (b1b)
    Compound 1 (2-chloro-6-fluorophenyl)methyl 2-[1-[2-[3,5- 200:1 to 2:1  50:1 to 2:1 25:1 to 4:1 
    bis(difluoromethyl)-1H-pyrazol-1-yl]acetyl]-
    4-piperidinyl]-4-thiazolecarboxylate (b2a)
    Compound 1 (1R)-1,2,3,4-tetrahydro-1-naphthalenyl 2-[1- 200:1 to 1:2  50:1 to 2:1 25:1 to 4:1 
    [2-[3,5-bis(difluoromethyl)-1H-pyrazol-1-
    yl]acetyl]-4-piperidinyl]-4-thiazolecarboxylate
    (b2b)
    Compound 1 [[4-methoxy-2-[[[(35,7R,8R,9S)-9-methyl-8- 200:1 to 1:2  50:1 to 2:1 25:1 to 4:1 
    (2-methyl-1-oxopropoxy)-2,6-dioxo-7-
    (phenylmethyl)-1,5-dioxonan-3-yl]amino]-
    carbonyl]-3-pyridinyl]oxy]methyl
    2-methylpropanoate (b3a)
    Compound 1 (3S,6S,7R,8R)-3-[[[3-(acetyloxy)-4-methoxy- 200:1 to 1:2  50:1 to 2:1 25:1 to 4:1 
    2-pyridinyl]carbonyl]amino]-6-methyl-4,9-
    dioxo-8-(phenylmethyl)-1,5-dioxonan-7-yl 2-
    methylpropanoate (b3b)
    Compound 1 (3S,6S,7R,8R)-3-[[[3-[(acetyloxy)methoxy]-4- 200:1 to 1:2  50:1 to 2:1 25:1 to 4:1 
    methoxy-2-pyridinyl]carbonyl]amino]-6-
    methyl-4,9-dioxo-8-(phenylmethyl)-1,5-
    dioxonan-7-yl 2-methylpropanoate (b3c)
    Compound 1 (3S,6S,7R,8R)-3-[[[4-methoxy-3-[[(2-methyl- 200:1 to 1:2  50:1 to 2:1 25:1 to 4:1 
    propoxy)carbonyl]oxy]-2-pyridinyl]-
    carbonyl]amino]-6-methyl-4,9-dioxo-
    8-(phenylmethyl)-1,5-dioxonan-7-yl
    2-methylpropanoate (b3d)
    Compound 1 N-[[3-(1,3-benzodioxol-5-ylmethoxy)-4- 200:1 to 1:2  50:1 to 2:1 25:1 to 4:1 
    methoxy-2-pyridinyl]carbonyl]-O-[2,5-
    dideoxy-3-O-(2-methyl-1-oxopropyl)-2-
    (phenylmethyl)-L-arabinonoyl]-L-serine,
    (1→4′)-lactone (b3e)
    Compound 1 5-fluoro-2-[(4-methylphenyl)methoxy]-4- 20:1 to 1:20  5:1 to 1:5 3:1 to 1:3
    pyrimidinamine (b4a)
    Compound 1 5-fluoro-2-[(4-fluorophenyl)methoxy]-4- 20:1 to 1:20  5:1 to 1:5 3:1 to 1:3
    pyrimidinamine (b4b)
    Compound 1 5,8-difluoro-N-[2-[3-methoxy-4-[[4- 40:1 to 1:10 10:1 to 1:3 5:1 to 1:2
    (trifluoromethyl)-2-pyridinyl]oxy]phenyl]-
    ethyl]-4-quinazolinamine (b5)
    Compound 1 pentyl [6-[[[(Z)-[(1-methyl-1H-tetrazol-5- 40:1 to 1:10 10:1 to 1:3 5:1 to 1:2
    yl)phenylmethylene]amino]oxy]methyl]-2-
    pyridinyl]carbamate (b6a)
    Compound 1 1,1-dimethylethyl N-[6-[[[(Z)-[(1-methyl-1H- 40:1 to 1:10 10:1 to 1:3 5:1 to 1:2
    tetrazol-5-yl)phenylmethylene]amino]oxy]-
    methyl]-2-pyridinyl]carbamate (b6b)
    Compound 1 3-butyn-1-yl N-[6-[[[(Z)-[(1-methyl-1H- 40:1 to 1:10 10:1 to 1:3 5:1 to 1:2
    tetrazol-5-yl)phenylmethylene]amino]oxy]-
    methyl]-2-pyridinyl]carbamate (b6c)
    Compound 1 N-(3′,4′-difluoro[1,1′-biphenyl]-2-yl)-3- 20:1 to 1:20  5:1 to 1:5 3:1 to 1:3
    (trifluoromethyl)-2-pyrazinecarboxamide (b7)
    Compound 1 N-[2-(2,4-dichlorophenyl)-2-methoxy-1- 20:1 to 1:20  5:1 to 1:5 3:1 to 1:3
    methylethyl]-3-(difluoromethyl)-1-methyl-
    2H-pyrazole-4-carboxamide (b8)
    Compound 1 3-(difluoromethyl)-N-[4-fluoro-2-(1,1,2,3,3,3- 20:1 to 1:20  5:1 to 1:5 3:1 to 1:3
    hexafluoropropoxy)phenyl]-1-methyl-1H-
    pyrazole-4-carboxamide (b9a)
    Compound 1 3-(difluoromethyl)-1-methyl-N-[2-(1,1,2,2- 20:1 to 1:20  5:1 to 1:5 3:1 to 1:3
    tetrafluoroethoxy)phenyl]-1H-pyrazole-4-
    carboxamide (b9b)
    Compound 1 isofetamid (b10a) 20:1 to 1:20  5:1 to 1:5 3:1 to 1:3
    Compound 1 tolprocarb (b10b) 20:1 to 1:20  5:1 to 1:5 3:1 to 1:3
    Compound 1 (αR)-2-[(2,5-dimethylphenoxy)methyl]-ex- 20:1 to 1:20  5:1 to 1:5 3:1 to 1:3
    methoxy-N-methylbenzeneacetamide (b11)
    Compound 1 2,6-dimethyl-1H,5H-[1,4]dithiino[2,3-c:5,6-  1:1 to 1:400   1:4 to 1:100  1:8 to 1:50
    c′]dipyrrole-1,3,5,7(2H,6H)-tetrone (b12)
    Compound 1 N-cyclopropyl-3-(difluoromthyl)-5-fluoro-1- 20:1 to 1:20  5:1 to 1:5 3:1 to 1:3
    methyl-N-[[2-(1-methylethyl)phenyl]methyl]-
    1H-pyrazole-4-carboxamide (b13)
  • Tables A2 through A13 are each constructed the same as Table A1 above except that entries below the “Component (a)” column heading are replaced with the respective Component (a) Column Entry shown below. Thus, for example, in Table A2 the entries below the “Component (a)” column heading all recite “Compound 2”, and the first line below the column headings in Table A2 specifically discloses combination of Compound 2 with 1-[4-[4-[5-(2,6-difluorophenyl)-4,5-dihydro-3-isoxazolyl]-2-thiazolyl]-1-piperidinyl]-2-[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]ethanone. Tables A3 through A13 are constructed similarly.
  • Table Number Component (a) Column Entry
    A2 Compound 2
    A3 Compound 3
    A4 Compound 4
    A5 Compound 5
    A6 Compound 6
    A7 Compound 7
    A8 Compound 8
    A9 Compound 9
    A10 Compound 10
    A11 Compound 11
    A12 Compound 12
    A13 Compound 13
  • Specific mixtures are listed in Tables B1 through B13. (Compound numbers refer to compounds in Index Table A, and Component (b) is identified in Table A1.) In Table B1, each line below the column headings “Component (a)” and “Component (b)” specifically discloses a mixture of Component (a), which is Compound 1, with a Component (b) fungicidal compound. The entries under the heading “Illustrative Ratios” disclose seven specific weight ratios of Component (a) relative to Component (b) for the disclosed mixture. For example, the first line of Table B1 discloses a mixture of Compound 1 with 1-[4-[4-[5-(2,6-difluorophenyl)-4,5-dihydro-3-isoxazolyl]-2-thiazolyl]-1-piperidinyl]-2-[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]ethanone (b1) and lists weight ratios of Compound 1 relative to Component (b1) of 2:1, 4:1, 8:1, 20:1, 50:1, 100:1 or 200:1. Table B1 thus supplements with specific ratios the general ranges of ratios for the combinations disclosed in Table A1.
  • TABLE B1
    Component Compo-
    (a) nent (b) Illustrative Ratios
    Compound 1 b1a 2:1 4:1  8:1 20:1  50:1 100:1 200:1
    Compound 1 b1aa 4:1 8:1 16:1 40:1 100:1 200:1 400:1
    Compound 1 b1b 2:1 4:1  8:1 20:1  50:1 100:1 200:1
    Compound 1 b2a 1:1 2:1  4:1 10:1  25:1  50:1 100:1
    Compound 1 b2b 1:1 2:1  4:1 10:1  25:1  50:1 100:1
    Compound 1 b3a 1:1 2:1  4:1 10:1  25:1  50:1 100:1
    Compound 1 b3b 1:1 2:1  4:1 10:1  25:1  50:1 100:1
    Compound 1 b3c 1:1 2:1  4:1 10:1  25:1  50:1 100:1
    Compound 1 b3d 1:1 2:1  4:1 10:1  25:1  50:1 100:1
    Compound 1 b3e 1:1 2:1  4:1 10:1  25:1  50:1 100:1
    Compound 1 b4a 1:10 1:5  1:3  1:1   3:1  5:1  10:1
    Compound 1 b4b 1:10 1:5  1:3  1:1   3:1  5:1  10:1
    Compound 1 b5 1:5 1:3  1:2  2:1   5:1  10:1  20:1
    Compound 1 b6a 1:5 1:3  1:2  2:1   5:1  10:1  20:1
    Compound 1 b6b 1:5 1:3  1:2  2:1   5:1  10:1  20:1
    Compound 1 b6c 1:5 1:3  1:2  2:1   5:1  10:1  20:1
    Compound 1 b7 1:10 1:5  1:3  1:1   3:1  5:1  10:1
    Compound 1 b8 1:10 1:5  1:3  1:1   3:1  5:1  10:1
    Compound 1 b9a 1:10 1:5  1:3  1:1   3:1  5:1  10:1
    Compound 1 b9b 1:10 1:5  1:3  1:1   3:1  5:1  10:1
    Compound 1 b10a 1:10 1:5  1:3  1:1   3:1  5:1  10:1
    Compound 1 b10b 1:10 1:5  1:3  1:1   3:1  5:1  10:1
    Compound 1 b11 1:10 1:5  1:3  1:1   3:1  5:1  10:1
    Compound 1 b12 1:200 1:100  1:50  1:18   1:8  1:4  1:2
    Compound 1 b13 1:10 1:5  1:3  1:1   3:1  5:1  10:1
  • Tables B2 through B13 are each constructed the same as Table B1 above except that entries below the “Component (a)” column heading are replaced with the respective Component (a) Column Entry shown below. Thus, for example, in Table B2 the entries below the “Component (a)” column heading all recite “Compound 2”, and the first line below the column headings in Table A2 specifically discloses a mixture of Compound 2 with 1-[4-[4-[5-(2,6-difluorophenyl)-4,5-dihydro-3-isoxazolyl]-2-thiazolyl]-1-piperidinyl]-2-[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]ethanone. Tables B3 through B13 are constructed similarly. Tables B2 through B13 thus supplement with specific ratios the general ranges of ratios for the combinations disclosed in Tables A2 through A13, respectively.
  • Table Number Component (a) Column Entry
    B2 Compound 2
    B3 Compound 3
    B4 Compound 4
    B5 Compound 5
    B6 Compound 6
    B7 Compound 7
    B8 Compound 8
    B9 Compound 9
    B10 Compound 10
    B11 Compound 11
    B12 Compound 12
    B13 Compound 13
  • As already noted, the present invention includes embodiments wherein the composition comprising components (a) and (b) further comprises as component (c) one or more biologically active compounds or agents. Therefore embodiments of the present composition include combinations of the mixtures disclosed in Tables A1 through A12 and B1 through B13 with additional biological compounds or agents. Of note as additional biological compounds or agents are fungicidal compounds selected from (c1) through (c46) already described. The weight ratio of component (c) to component (a) is generally between about 1:3000 and about 3000:1, more typically between about 1:500 and about 500:1, between about 125:1 and about 1:125, and between about 25:1 and 1:25 and most typically between about 5:1 and about 1:5. One skilled in the art can easily determine through simple experimentation the weight ratios and application rates of fungicidal compounds necessary for the desired spectrum of plant disease protection and control.
  • Table C lists typical, more typical, and most typical weight ratios for specific component (c) fungicides relative to component (a) in compositions comprising components (a) and (c) either before (i.e. without component (b)) or after inclusion of component (b).
  • TABLE C
    More Most
    Typical Typical Typical Illustrative
    Weight Weight Weight Weight
    Component (c) Ratio Ratio Ratio Ratio
    acibenzolar-S-methyl   2:1 to 1:180  1:1 to 1:60  1:1 to 1:18 1:4
    aldimorph 30:1 to 1:3 10:1 to 1:1  7:1 to 1:1 3:1
    ametoctradin  9:1 to 1:18 3:1 to 1:6 3:1 to 1:3 1:1
    amisulbrom  6:1 to 1:18 2:1 to 1:6 1:1 to 1:6 1:2
    anilazine 90:1 to 2:1 30:1 to 4:1  22:1 to 4:1  8:1
    azaconazole  7:1 to 1:18 2:1 to 1:6 2:1 to 1:4 1:2
    azoxystrobin  9:1 to 1:12 3:1 to 1:4 3:1 to 1:3 1:1
    benalaxyl  4:1 to 1:18 1:1 to 1:6 1:1 to 1:6 1:2
    benalaxyl-M  4:1 to 1:36  1:1 to 1:12 1:1 to 1:8 1:3
    benodanil 18:1 to 1:6 6:1 to 1:2 4:1 to 1:2 2:1
    benomyl 45:1 to 1:4 15:1 to 1:1  11:1 to 1:1  4:1
    benthiavalicarb or  2:1 to 1:36  1:1 to 1:12  1:1 to 1:12 1:4
    benthiavalicarb-isopropyl
    bethoxazin 150:1 to 1:36 50:1 to 1:12 15:1 to 2:1  5:1
    binapacryl 150:1 to 1:36 50:1 to 1:12 15:1 to 2:1  5:1
    biphenyl 150:1 to 1:36 50:1 to 1:12 15:1 to 2:1  5:1
    bitertanol 15:1 to 1:5 5:1 to 1:2 3:1 to 1:2 1:1
    bixafen 12:1 to 1:9 4:1 to 1:3 2:1 to 1:3 1:1
    blasticidin-S  3:1 to 1:90  1:1 to 1:30  1:4 to 1:30  1:12
    boscalid 18:1 to 1:6 6:1 to 1:2 4:1 to 1:2 2:1
    bromuconazole 15:1 to 1:9 5:1 to 1:3 3:1 to 1:3 1:1
    bupirimate  3:1 to 1:90  1:1 to 1:30  1:3 to 1:30  1:10
    captafol 90:1 to 1:4 30:1 to 1:2  15:1 to 2:1  5:1
    captan 90:1 to 1:4 30:1 to 1:2  15:1 to 2:1  5:1
    carbendazim 45:1 to 1:4 15:1 to 1:2  11:1 to 2:1  4:1
    carboxin 18:1 to 1:6 6:1 to 1:2 4:1 to 1:2 2:1
    carpropamid 15:1 to 1:9 5:1 to 1:3 3:1 to 1:3 1:1
    chloroneb 300:1 to 2:1  100:1 to 4:1  100:1 to 14:1  35:1 
    chlorothalonil 90:1 to 1:4 30:1 to 1:2  15:1 to 2:1  5:1
    chlozolinate 45:1 to 1:2 15:1 to 2:1  11:1 to 2:1  4:1
    clotrimazole 15:1 to 1:9 5:1 to 1:3 3:1 to 1:3 1:1
    copper salts such as Bordeaux mixture 450:1 to 1:1  150:1 to 4:1  45:1 to 5:1  15:1 
    (tribasic copper sulfate), copper oxychloride,
    copper sulfate and copper hydroxide
    cyazofamid  4:1 to 1:18 1:1 to 1:6 1:1 to 1:6 1:2
    cyflufenamid  1:1 to 1:90  1:2 to 1:30  1:2 to 1:24 1:6
    cymoxanil  6:1 to 1:18 2:1 to 1:6 1:1 to 1:5 1:2
    cyproconazole  4:1 to 1:18 1:1 to 1:6 1:1 to 1:6 1:2
    cyprodinil 22:1 to 1:9 7:1 to 1:3 4:1 to 1:2 2:1
    dichlofluanid 150:1 to 1:36 50:1 to 1:12 15:1 to 2:1  5:1
    diclocymet 150:1 to 1:36 50:1 to 1:12 15:1 to 2:1  5:1
    diclomezine 15:1 to 1:9 5:1 to 1:3 3:1 to 1:3 1:1
    dicloran 150:1 to 1:36 50:1 to 1:12 15:1 to 2:1  5:1
    diethofencarb 22:1 to 1:9 7:1 to 1:3 7:1 to 1:2 2:1
    difenoconazole  4:1 to 1:36  1:1 to 1:12  1:1 to 1:12 1:3
    diflumetorim 150:1 to 1:36 50:1 to 1:12 15:1 to 2:1  5:1
    dimethirimol  3:1 to 1:90  1:1 to 1:30  1:3 to 1:30 1:8
    dimethomorph  9:1 to 1:6 3:1 to 1:2 3:1 to 1:2 1:1
    dimoxystrobin  9:1 to 1:18 3:1 to 1:6 2:1 to 1:4 1:1
    diniconazole  3:1 to 1:36  1:1 to 1:12 1:1 to 1:8 1:3
    diniconazole M  3:1 to 1:90  1:1 to 1:30  1:1 to 1:12 1:3
    dinocap  7:1 to 1:9 2:1 to 1:3 2:1 to 1:3 1:1
    dithianon 15:1 to 1:4 5:1 to 1:2 5:1 to 1:2 2:1
    dodemorph 30:1 to 1:3 10:1 to 1:1  7:1 to 1:1 3:1
    dodine 30:1 to 1:2 10:1 to 2:1  10:1 to 2:1  4:1
    edifenphos 30:1 to 1:9 10:1 to 1:3  3:1 to 1:3 1:1
    enestroburin  9:1 to 1:18 3:1 to 1:6 2:1 to 1:4 1:1
    epoxiconazole  3:1 to 1:36  1:1 to 1:12 1:1 to 1:7 1:3
    etaconazole  3:1 to 1:36  1:1 to 1:12 1:1 to 1:7 1:3
    ethaboxam  7:1 to 1:9 2:1 to 1:3 2:1 to 1:3 1:1
    ethirimol 30:1 to 1:3 10:1 to 1:1  7:1 to 1:1 3:1
    etridiazole 30:1 to 1:9 10:1 to 1:3  7:1 to 1:2 2:1
    famoxadone  9:1 to 1:18 3:1 to 1:6 2:1 to 1:4 1:1
    fenamidone  6:1 to 1:18 2:1 to 1:6 2:1 to 1:4 1:1
    fenarimol  3:1 to 1:90  1:1 to 1:30  1:2 to 1:24 1:7
    fenbuconazole  3:1 to 1:30  1:1 to 1:10  1:1 to 1:10 1:3
    fenfuram 18:1 to 1:6 6:1 to 1:2 4:1 to 1:2 1:1
    fenhexamid 30:1 to 1:2 10:1 to 2:1  10:1 to 2:1  4:1
    fenoxanil 150:1 to 1:36 50:1 to 1:12 15:1 to 1:1  4:1
    fenpiclonil 75:1 to 1:9 25:1 to 1:3  15:1 to 2:1  5:1
    fenpropidin 30:1 to 1:3 10:1 to 1:1  7:1 to 1:1 2:1
    fenpropimorph 30:1 to 1:3 10:1 to 1:1  7:1 to 1:1 2:1
    fenpyrazamine  100:1 to 1:100 10:1 to 1:10 3:1 to 1:3 1:1
    fentin salt such as the acetate, chloride or 15:1 to 1:9 5:1 to 1:3 3:1 to 1:3 1:1
    hydroxide
    ferbam 300:1 to 1:2  100:1 to 2:1  30:1 to 4:1  10:1 
    ferimzone 30:1 to 1:5 10:1 to 1:2  7:1 to 1:2 2 1
    fluazinam 22:1 to 1:5 7:1 to 1:2 3:1 to 1:2 1 1
    fludioxonil  7:1 to 1:12 2:1 to 1:4 2:1 to 1:4 1 1
    flumetover  9:1 to 1:6 3:1 to 1:2 3:1 to 1:2 1 1
    flumorph  9:1 to 1:18 3:1 to 1:6 3:1 to 1:3 1 1
    fluopicolide  3:1 to 1:18 1:1 to 1:6 1:1 to 1:6 12
    fluopyram  15:1 to 1:90  5:1 to 1:30 3:1 to 1:3 1 1
    fluoromide 150:1 to 2:1  50:1 to 4:1  37:1 to 5:1  14:1 
    fluoxastrobin  4:1 to 1:18 1:1 to 1:6 1:1 to 1:6 1:2
    fluquinconazole  4:1 to 1:12 1:1 to 1:4 1:1 to 1:4 1:2
    flusilazole 15:1 to 1:9 5:1 to 1:3 3:1 to 1:3 1:1
    flusulfamide 90:1 to 1:2 30:1 to 2:1  15:1 to 2:1  5:1
    flutianil  7:1 to 1:36  2:1 to 1:12 1:1 to 1:6 1:2
    flutolanil 18:1 to 1:6 6:1 to 1:2 4:1 to 1:2 1:1
    flutriafol  4:1 to 1:12 1:1 to 1:4 1:1 to 1:4 1:2
    fluxapyroxad 12:1 to 1:9 4:1 to 1:3 2:1 to 1:3 1:1
    folpet 90:1 to 1:4 30:1 to 1:2  15:1 to 2:1  5:1
    fosetyl-aluminum 225:1 to 2:1  75:1 to 5:1  30:1 to 5:1  12:1 
    fuberidazole 45:1 to 1:4 15:1 to 1:2  11:1 to 2:1  4:1
    furalaxyl  15:1 to 1:45  5:1 to 1:15 1:1 to 1:6 1:2
    furametpyr 150:1 to 1:36 50:1 to 1:12 15:1 to 2:1  5:1
    guazatine or iminoctadine 150:1 to 1:36 50:1 to 1:12 15:1 to 2:1  5:1
    hexaconazole  15:1 to 1:36  5:1 to 1:12 1:1 to 1:5 1:2
    hymexazol 225:1 to 2:1  75:1 to 4:1  75:1 to 9:1  25:1 
    imazalil  7:1 to 1:18 2:1 to 1:6 1:1 to 1:5 1:2
    imibenconazole  15:1 to 1:36  5:1 to 1:12 1:1 to 1:5 1:2
    iodocarb 150:1 to 1:36 50:1 to 1:12 15:1 to 2:1  4:1
    ipconazole  15:1 to 1:36  5:1 to 1:12 1:1 to 1:5 1:2
    iprobenfos 150:1 to 1:36 50:1 to 1:12 15:1 to 2:1  5:1
    iprodione 120:1 to 1:2  40:1 to 2:1  15:1 to 2:1  5:1
    iprovalicarb  9:1 to 1:9 3:1 to 1:3 2:1 to 1:3 1:1
    isoprothiolane 150:1 to 2:1  50:1 to 4:1  45:1 to 5:1  15:1 
    isopyrazam 12:1 to 1:9 4:1 to 1:3 2:1 to 1:3 1:1
    isotianil 12:1 to 1:9 4:1 to 1:3 2:1 to 1:3 1:1
    kasugamycin  7:1 to 1:90  2:1 to 1:30  1:2 to 1:24 1:7
    kresoxim-methyl  7:1 to 1:18 2:1 to 1:6 2:1 to 1:4 1:1
    mancozeb 180:1 to 1:3  60:1 to 2:1  22:1 to 3:1  7:1
    mandipropamid  6:1 to 1:18 2:1 to 1:6 2:1 to 1:4 1:1
    maneb 180:1 to 1:3  60:1 to 2:1  22:1 to 3:1  7:1
    mepanipyrim 18:1 to 1:3 6:1 to 1:1 6:1 to 1:1 2:1
    mepronil  7:1 to 1:36  2:1 to 1:12 1:1 to 1:6 1:2
    meptyldinocap  7:1 to 1:9 2:1 to 1:3 2:1 to 1:3 1:1
    metalaxyl  15:1 to 1:45  5:1 to 1:15 1:1 to 1:6 1:2
    metalaxyl-M  7:1 to 1:90  2:1 to 1:30  1:1 to 1:12 1:4
    metconazole  3:1 to 1:18 1:1 to 1:6 1:1 to 1:6 1:2
    methasulfocarb 150:1 to 1:36 50:1 to 1:12 15:1 to 1:1  5:1
    metiram 150:1 to 1:36 50:1 to 1:12 15:1 to 1:1  5:1
    metominostrobin  9:1 to 1:12 3:1 to 1:4 3:1 to 1:3 1:1
    metrafenone  6:1 to 1:12 2:1 to 1:4 2:1 to 1:4 1:1
    myclobutanil  5:1 to 1:26 1:1 to 1:9 1:1 to 1:8 1:3
    naftifine 150:1 to 1:36 50:1 to 1:12 15:1 to 2:1  5:1
    neo-asozin (ferric methanearsonate) 150:1 to 1:36 50:1 to 1:12 15:1 to 2:1  5:1
    nuarimol 15:1 to 1:9 5:1 to 1:3 3:1 to 1:3 1:1
    octhilinone 150:1 to 1:36 50:1 to 1:12 15:1 to 1:1  4:1
    ofurace  15:1 to 1:45  5:1 to 1:15 1:1 to 1:6 1:2
    orysastrobin  9:1 to 1:12 3:1 to 1:4 3:1 to 1:3 1:1
    oxadixyl  15:1 to 1:45  5:1 to 1:15 1:1 to 1:6 1:2
    oxolinic acid 30:1 to 1:9 10:1 to 1:3  7:1 to 1:2 2:1
    oxpoconazole  15:1 to 1:36  5:1 to 1:12 1:1 to 1:5 1:2
    oxycarboxin 18:1 to 1:6 6:1 to 1:2 4:1 to 1:2 1:1
    oxytetracycline 15:1 to 1:9 5:1 to 1:3 3:1 to 1:3 1:1
    pefurazoate 150:1 to 1:36 50:1 to 1:12 15:1 to 2:1  5:1
    penconazole  1:1 to 1:45  1:2 to 1:15  1:2 to 1:15 1:6
    pencycuron 150:1 to 1:2  50:1 to 2:1  11:1 to 2:1  4:1
    penflufen 12:1 to 1:9 4:1 to 1:3 2:1 to 1:3 1:1
    penthiopyrad 12:1 to 1:9 4:1 to 1:3 2:1 to 1:3 1:1
    phosphorous acid and salts thereof 150:1 to 1:36 50:1 to 1:12 15:1 to 2:1  6:1
    phthalide 150:1 to 1:36 50:1 to 1:12 15:1 to 2:1  6:1
    picoxystrobin  7:1 to 1:18 2:1 to 1:6 1:1 to 1:5 1:2
    piperalin 15:1 to 1:9 5:1 to 1:3 3:1 to 1:3 1:1
    polyoxin 15:1 to 1:9 5:1 to 1:3 3:1 to 1:3 1:1
    probenazole 15:1 to 1:9 5:1 to 1:3 3:1 to 1:3 1:1
    prochloraz 22:1 to 1:4 7:1 to 1:1 7:1 to 1:2 2:1
    procymidone 45:1 to 1:3 15:1 to 1:1  11:1 to 2:1  4:1
    propamocarb or propamocarb-hydrochloride 30:1 to 1:2 10:1 to 2:1  10:1 to 2:1  4:1
    propiconazole  4:1 to 1:18 1:1 to 1:6 1:1 to 1:5 1:2
    propineb 45:1 to 1:2 15:1 to 2:1  11:1 to 2:1  4:1
    proquinazid  3:1 to 1:36  1:1 to 1:12  1:1 to 1:12 1:3
    prothiocarb  9:1 to 1:18 3:1 to 1:6 3:1 to 1:3 1:1
    prothioconazole  6:1 to 1:18 2:1 to 1:6 1:1 to 1:5 1:2
    pyraclostrobin  9:1 to 1:18 3:1 to 1:6 2:1 to 1:4 1:1
    pyrametostrobin  9:1 to 1:18 3:1 to 1:6 2:1 to 1:4 1:1
    pyraoxystrobin  9:1 to 1:18 3:1 to 1:6 2:1 to 1:4 1:1
    pyrazophos 150:1 to 1:36 50:1 to 1:12 15:1 to 1:1  4:1
    pyribencarb 15:1 to 1:6 5:1 to 1:2 4:1 to 1:2 1:1
    pyrifenox 15:1 to 1:9 5:1 to 1:3 3:1 to 1:3 1:1
    pyrimethanil 30:1 to 1:6 10:1 to 1:2  3:1 to 1:2 1:1
    pyriofenone  6:1 to 1:12 2:1 to 1:4 2:1 to 1:4 1:1
    pyroquilon 15:1 to 1:9 5:1 to 1:3 3:1 to 1:3 1:1
    pyrrolnitrin 150:1 to 1:36 50:1 to 1:12 15:1 to 2:1  5:1
    quinconazole  4:1 to 1:12 1:1 to 1:4 1:1 to 1:4 1:2
    quinomethionate 150:1 to 1:36 50:1 to 1:12 15:1 to 2:1  5:1
    quinoxyfen  4:1 to 1:18 1:1 to 1:6 1:1 to 1:6 1:2
    quintozene 150:1 to 1:36 50:1 to 1:12 15:1 to 2:1  5:1
    silthiofam  7:1 to 1:18 2:1 to 1:6 2:1 to 1:4 1:1
    simeconazole  15:1 to 1:36  5:1 to 1:12 1:1 to 1:5 1:2
    spiroxamine 22:1 to 1:4 7:1 to 1:2 5:1 to 1:2 2:1
    streptomycin 15:1 to 1:9 5:1 to 1:3 3:1 to 1:3 1:1
    sulfur 300:1 to 3:1  100:1 to 9:1  75:1 to 9:1  25:1 
    tebuconazole  7:1 to 1:18 2:1 to 1:6 1:1 to 1:5 1:2
    tebufloquin  100:1 to 1:100 10:1 to 1:10 3:1 to 1:3 1:1
    tecloftalam 150:1 to 1:36 50:1 to 1:12 15:1 to 2:1  5:1
    tecnazene 150:1 to 1:36 50:1 to 1:12 15:1 to 2:1  5:1
    terbinafine 150:1 to 1:36 50:1 to 1:12 15:1 to 2:1  5:1
    tetraconazole  15:1 to 1:36  5:1 to 1:12 1:1 to 1:5 1:2
    thiabendazole 45:1 to 1:4 15:1 to 1:2  11:1 to 2:1  4:1
    thifluzamide 15:1 to 1:9 5:1 to 1:3 3:1 to 1:3 1:1
    thiophanate 45:1 to 1:3 15:1 to 2:1  11:1 to 2:1  4:1
    thiophanate-methyl 45:1 to 1:3 15:1 to 2:1  11:1 to 2:1  4:1
    thiram 150:1 to 1:2  50:1 to 2:1  37:1 to 5:1  14:1 
    tiadinil 12:1 to 1:9 4:1 to 1:3 2:1 to 1:3 1:1
    tolclofos-methyl 150:1 to 1:2  50:1 to 2:1  37:1 to 5:1  14:1 
    tolylfluanid 150:1 to 1:36 50:1 to 1:12 15:1 to 2:1  5:1
    triadimefon  15:1 to 1:36  5:1 to 1:12 1:1 to 1:5 1:2
    triadimenol  15:1 to 1:36  5:1 to 1:12 1:1 to 1:5 1:2
    triarimol  3:1 to 1:90  1:1 to 1:30  1:2 to 1:24 1:7
    triazoxide 150:1 to 1:36 50:1 to 1:12 15:1 to 2:1  5:1
    tricyclazole 15:1 to 1:9 5:1 to 1:3 3:1 to 1:3 1:1
    tridemorph 30:1 to 1:3 10:1 to 1:1  7:1 to 1:1 2:1
    trifloxystrobin  6:1 to 1:18 2:1 to 1:6 2:1 to 1:4 1:1
    triflumizole 15:1 to 1:9 5:1 to 1:3 3:1 to 1:3 1:1
    triforine 15:1 to 1:9 5:1 to 1:3 3:1 to 1:3 1:1
    trimorphamide 45:1 to 1:9 15:1 to 1:3  7:1 to 1:2 2 1
    triticonazole  15:1 to 1:36  5:1 to 1:12 1:1 to 1:5 12
    uniconazole  15:1 to 1:36  5:1 to 1:12 1:1 to 1:5 12
    validamycin 150:1 to 1:36 50:1 to 1:12 3:1 to 1:3 1 1
    valifenalate  6:1 to 1:18 2:1 to 1:6 2:1 to 1:4 1 1
    vinclozolin 120:1 to 1:2  40:1 to 2:1  15:1 to 2:1  6 1
    zineb 150:1 to 1:2  50:1 to 2:1  37:1 to 5:1  14:1 
    ziram 150:1 to 1:2  50:1 to 2:1  37:1 to 5:1  14:1 
    zoxamide  6:1 to 1:18 2:1 to 1:6 2:1 to 1:4 1:1
    5-chloro-6-(2,4,6-trifluorophenyl)-  15:1 to 1:36  5:1 to 1:12 1:1 to 1:6 1:2
    7-(4-methylpiperidin-1-yl)[1,2,4]triazolo[1,5-
    a]pyrimidine
    N-[2-[4-[[3-(4-chlorophenyl)-2-propyn-  6:1 to 1:18 2:1 to 1:6 2:1 to 1:4 1:1
    1-yl]oxy]-3-methoxyphenyl]ethyl]-3-methyl-
    2-[(methylsulfonyl)amino]butanamide
    N-[2-[4-[[3-(4-chlorophenyl)-2-propyn-1-  6:1 to 1:18 2:1 to 1:6 2:1 to 1:4 1:1
    yl]oxy]-3-methoxyphenyl]ethyl]-3-methyl-2-
    [(ethylsulfonyl)amino]butanamide
    2-butoxy-6-iodo-3-propyl-4H-1-benzopyran-  3:1 to 1:36  1:1 to 1:12  1:1 to 1:12 1:3
    4-one
    3-[5-(4-chlorophenyl)-2,3-dimethyl-3- 15:1 to 1:9 5:1 to 1:3 3:1 to 1:3 1:1
    isoxazolidinyl]pyridine
    N′-[4-[[3-[(4-chlorophenyl)methyl]-1,2,4-  20:1 to 1:20 8:1 to 1:8 3:1 to 1:3 1:1
    thiadiazol-5-yl]oxy]-2,5-dimethylphenyl]-N-
    ethyl-N-methylmethanimidamide
    4-fluorophenyl N-[1-[[[1-(4-cyanophenyl)-  6:1 to 1:18 2:1 to 1:6 2:1 to 1:4 1:1
    ethyl]sulfonyl]methyl]propyl]carbamate
    N-[[(cyclopropylmethoxy)amino][6-  1:1 to 1:90  1:2 to 1:30  1:2 to 1:24 1:7
    (difluoromethoxy)-2,3-difluorophenyl]-
    methylene]benzeneacetamide
    α-[methoxyimino]-N-methyl-2-[[[1-[3-  9:1 to 1:18 3:1 to 1:6 3:1 to 1:3 1:1
    (trifluoromethyl)phenyl]ethoxy]imino]-
    methyl]benzeneacetamide
    N′-[4-[4-chloro-3-(trifluoromethyl)phenoxy]-  15:1 to 1:18 5:1 to 1:6 3:1 to 1:3 1:1
    2,5-dimethylphenyl]-N-ethyl-
    N-methylmethanimidamide
    N-(4-chloro-2-nitrophenyl)-N-ethyl-  15:1 to 1:18 5:1 to 1:6 3:1 to 1:3 1:1
    4-methylbenzenesulfonamide
    2-[[[3-(2,6-dichlorophenyl)-1-methyl-  9:1 to 1:18 3:1 to 1:6 3:1 to 1:3 1:1
    2-propen-1-ylidene]amino]oxy]methyl]-
    α-(methoxyimino)-
    N-methylbenzeneacetamide
    pentyl N-[4-[[[[(1-methyl-1H-tetrazol-5-yl)-  9:1 to 1:18 3:1 to 1:6 3:1 to 1:3 1:1
    phenylmethylene]amino]oxy]methyl]-2-
    thiazolyl]carbamate
    pentyl N-[6-[[[[(1-methyl-1H-tetrazol-5-yl)-  9:1 to 1:18 3:1 to 1:6 3:1 to 1:3 1:1
    phenylmethylene]amino]oxy]methyl]-2-
    pyridinyl]carbamate
    2-[(3-bromo-6-quinolinyl)oxy]-  5:1 to 1:22 2:1 to 1:8 2:1 to 1:4 1:1
    N-(1,1-dimethyl-2-butyn-1-yl)-
    2-(methylthio)acetamide
    2-[(3-ethynyl-6-quinolinyl)oxy]-  5:1 to 1:22 2:1 to 1:8 2:1 to 1:4 1:1
    N-[1-(hydroxymethyl)-1-methyl-2-propyn-1-
    yl]-2-(methylthio)acetamide
    N-(1,1-dimethyl-2-butyn-1-yl)-2-[(3-ethynyl-  5:1 to 1:22 2:1 to 1:8 2:1 to 1:4 1:1
    6-quinolinyl)oxy]-2-(methylthio)acetamide
  • The particular weight ratios defining the weight ratio ranges in Table C constitute disclosure of specific weight ratios. Table C also specifically discloses an additional illustrative weight ratio. Illustrative of specific combinations of components (a), (b) and (c) in the compositions of the present invention are specific combinations and weight ratios of components (a) and (b) listed in Tables B1 through B13 further combined with particular component (c) fungicidal compounds in the specific weight ratios disclosed in Table C.
    • Formulation/Utility
  • A compound selected from compounds of Formula 1, N-oxides, and salts thereof, or a mixture (i.e. composition) comprising the compound with (b) at least one fungicidal compound selected from (b1) through (b13) and salts thereof as described in the Summary of the Invention, will generally be used to provide fungicidal active ingredients in further compositions, i.e. formulations, with at least one additional component selected from the group consisting of surfactants, solid diluents and liquid diluents, which serves as a carrier. The formulation or composition ingredients are selected to be consistent with the physical properties of the active ingredients, mode of application and environmental factors such as soil type, moisture and temperature.
  • The mixtures of component (a) (i.e. at least one compound of Formula 1, N-oxides, or salts thereof) with component (b) (e.g., selected from (b1) to (b13) and salts thereof as described above) and/or one or more other biologically active compounds or agents (i.e. insecticides, other fungicides, nematocides, acaricides, herbicides and other biological agents) can be formulated in a number of ways, including:
      • (i) component (a), component (b) and optionally (c) one or more other biologically active compounds or agents can be formulated separately and applied separately or applied simultaneously in an appropriate weight ratio, e.g., as a tank mix; or
      • (ii) component (a), component (b) and optionally (c) one or more other biologically active compounds or agents can be formulated together in the proper weight ratio.
  • Useful formulations include both liquid and solid compositions. Liquid compositions include solutions (including emulsifiable concentrates), suspensions, emulsions (including microemulsions and/or suspoemulsions) and the like, which optionally can be thickened into gels. The general types of aqueous liquid compositions are soluble concentrate, suspension concentrate, capsule suspension, concentrated emulsion, microemulsion and suspo-emulsion. The general types of nonaqueous liquid compositions are emulsifiable concentrate, microemulsifiable concentrate, dispersible concentrate and oil dispersion.
  • The general types of solid compositions are dusts, powders, granules, pellets, prills, pastilles, tablets, filled films (including seed coatings) and the like, which can be water-dispersible (“wettable”) or water-soluble. Films and coatings formed from film-forming solutions or flowable suspensions are particularly useful for seed treatment. Active ingredient can be (micro)encapsulated and further formed into a suspension or solid formulation; alternatively the entire formulation of active ingredient can be encapsulated (or “overcoated”). Encapsulation can control or delay release of the active ingredient. An emulsifiable granule combines the advantages of both an emulsifiable concentrate formulation and a dry granular formulation. High-strength compositions are primarily used as intermediates for further formulation.
  • Of note is a composition embodiment wherein granules of a solid composition comprising a compound of Formula 1 (or an N-oxide or salt thereof) is mixed with granules of a solid composition comprising component (b). These mixtures can be further mixed with granules comprising one or more additional biologically active compounds or agents, e.g., additional agricultural protectants. Alternatively, two or more agricultural protectants (e.g., a component (a) (Formula 1) compound, a component (b) compound, (c) an agricultural protectant other than component (a) or (b)) can be combined in the solid composition of one set of granules, which is then mixed with one or more sets of granules of solid compositions comprising one or more additional agricultural protectants. These granule mixtures can be in accordance with the general granule mixture disclosure of PCT Patent Publication WO 94/24861 or more preferably the homogeneous granule mixture teaching of U.S. Pat. No. 6,022,552.
  • Sprayable formulations are typically extended in a suitable medium before spraying. Such liquid and solid formulations are formulated to be readily diluted in the spray medium, usually water. Spray volumes can range from about from about one to several thousand liters per hectare, but more typically are in the range from about ten to several hundred liters per hectare. Sprayable formulations can be tank mixed with water or another suitable medium for foliar treatment by aerial or ground application, or for application to the growing medium of the plant. Liquid and dry formulations can be metered directly into drip irrigation systems or metered into the furrow during planting. Liquid and solid formulations can be applied onto seeds of crops and other desirable vegetation as seed treatments before planting to protect developing roots and other subterranean plant parts and/or foliage through systemic uptake.
  • The formulations will typically contain effective amounts of active ingredient, diluent and surfactant within the following approximate ranges which add up to 100 percent by weight.
  • Weight Percent
    Active
    Ingredient Diluent Surfactant
    Water-Dispersible and Water- 0.001-90 0-99.999 0-15
    soluble Granules, Tablets and
    Powders
    Oil Dispersions, Suspensions,    1-50 40-99    0-50
    Emulsions, Solutions
    (including Emulsifiable
    Concentrates)
    Dusts    1-25 70-99    0-5 
    Granules and Pellets 0.001-99 5-99.999 0-15
    High Strength Compositions   90-99 0-10    0-2 
  • Solid diluents include, for example, clays such as bentonite, montmorillonite, attapulgite and kaolin, gypsum, cellulose, titanium dioxide, zinc oxide, starch, dextrin, sugars (e.g., lactose, sucrose), silica, talc, mica, diatomaceous earth, urea, calcium carbonate, sodium carbonate and bicarbonate, and sodium sulfate. Typical solid diluents are described in Watkins et al., Handbook of Insecticide Dust Diluents and Carriers, 2nd Ed., Dorland Books, Caldwell, N.J.
  • Liquid diluents include, for example, water, N,N-dimethylalkanamides (e.g., N,N-dimethylformamide), limonene, dimethyl sulfoxide, N-alkylpyrrolidones (e.g., N-methylpyrrolidinone), ethylene glycol, triethylene glycol, propylene glycol, dipropylene glycol, polypropylene glycol, propylene carbonate, butylene carbonate, paraffins (e.g., white mineral oils, normal paraffins, isoparaffins), alkylbenzenes, alkylnaphthalenes, glycerine, glycerol triacetate, sorbitol, triacetin, aromatic hydrocarbons, dearomatized aliphatics, alkylbenzenes, alkylnaphthalenes, ketones such as cyclohexanone, 2-heptanone, isophorone and 4-hydroxy-4-methyl-2-pentanone, acetates such as isoamyl acetate, hexyl acetate, heptyl acetate, octyl acetate, nonyl acetate, tridecyl acetate and isobornyl acetate, other esters such as alkylated lactate esters, dibasic esters and γ-butyrolactone, and alcohols, which can be linear, branched, saturated or unsaturated, such as methanol, ethanol, n-propanol, isopropyl alcohol, n-butanol, isobutyl alcohol, n-hexanol, 2-ethylhexanol, n-octanol, decanol, isodecyl alcohol, isooctadecanol, cetyl alcohol, lauryl alcohol, tridecyl alcohol, oleyl alcohol, cyclohexanol, tetrahydrofurfuryl alcohol, diacetone alcohol and benzyl alcohol. Liquid diluents also include glycerol esters of saturated and unsaturated fatty acids (typically C6-C22), such as plant seed and fruit oils (e.g., oils of olive, castor, linseed, sesame, corn (maize), peanut, sunflower, grapeseed, safflower, cottonseed, soybean, rapeseed, coconut and palm kernel), animal-sourced fats (e.g., beef tallow, pork tallow, lard, cod liver oil, fish oil), and mixtures thereof. Liquid diluents also include alkylated fatty acids (e.g., methylated, ethylated, butylated) wherein the fatty acids may be obtained by hydrolysis of glycerol esters from plant and animal sources, and can be purified by distillation. Typical liquid diluents are described in Marsden, Solvents Guide, 2nd Ed., Interscience, New York, 1950.
  • The solid and liquid compositions of the present invention often include one or more surfactants. When added to a liquid, surfactants (also known as “surface-active agents”) generally modify, most often reduce, the surface tension of the liquid. Depending on the nature of the hydrophilic and lipophilic groups in a surfactant molecule, surfactants can be useful as wetting agents, dispersants, emulsifiers or defoaming agents.
  • Surfactants can be classified as nonionic, anionic or cationic. Nonionic surfactants useful for the present compositions include, but are not limited to: alcohol alkoxylates such as alcohol alkoxylates based on natural and synthetic alcohols (which may be branched or linear) and prepared from the alcohols and ethylene oxide, propylene oxide, butylene oxide or mixtures thereof; amine ethoxylates, alkanolamides and ethoxylated alkanolamides; alkoxylated triglycerides such as ethoxylated soybean, castor and rapeseed oils; alkylphenol alkoxylates such as octylphenol ethoxylates, nonylphenol ethoxylates, dinonyl phenol ethoxylates and dodecyl phenol ethoxylates (prepared from the phenols and ethylene oxide, propylene oxide, butylene oxide or mixtures thereof); block polymers prepared from ethylene oxide or propylene oxide and reverse block polymers where the terminal blocks are prepared from propylene oxide; ethoxylated fatty acids; ethoxylated fatty esters and oils; ethoxylated methyl esters; ethoxylated tristyrylphenol (including those prepared from ethylene oxide, propylene oxide, butylene oxide or mixtures thereof); fatty acid esters, glycerol esters, lanolin-based derivatives, polyethoxylate esters such as polyethoxylated sorbitan fatty acid esters, polyethoxylated sorbitol fatty acid esters and polyethoxylated glycerol fatty acid esters; other sorbitan derivatives such as sorbitan esters; polymeric surfactants such as random copolymers, block copolymers, alkyd peg (polyethylene glycol) resins, graft or comb polymers and star polymers; polyethylene glycols (pegs); polyethylene glycol fatty acid esters; silicone-based surfactants; and sugar-derivatives such as sucrose esters, alkyl polyglycosides and alkyl polysaccharides.
  • Useful anionic surfactants include, but are not limited to: alkylaryl sulfonic acids and their salts; carboxylated alcohol or alkylphenol ethoxylates; diphenyl sulfonate derivatives; lignin and lignin derivatives such as lignosulfonates; maleic or succinic acids or their anhydrides; olefin sulfonates; phosphate esters such as phosphate esters of alcohol alkoxylates, phosphate esters of alkylphenol alkoxylates and phosphate esters of styryl phenol ethoxylates; protein-based surfactants; sarcosine derivatives; styryl phenol ether sulfate; sulfates and sulfonates of oils and fatty acids; sulfates and sulfonates of ethoxylated alkylphenols; sulfates of alcohols; sulfates of ethoxylated alcohols; sulfonates of amines and amides such as N,N-alkyltaurates; sulfonates of benzene, cumene, toluene, xylene, and dodecyl and tridecylbenzenes; sulfonates of condensed naphthalenes; sulfonates of naphthalene and alkyl naphthalene; sulfonates of fractionated petroleum; sulfosuccinamates; and sulfosuccinates and their derivatives such as dialkyl sulfosuccinate salts.
  • Useful cationic surfactants include, but are not limited to: amides and ethoxylated amides; amines such as N-alkyl propanediamines, tripropylenetriamines and dipropylenetetramines, and ethoxylated amines, ethoxylated diamines and propoxylated amines (prepared from the amines and ethylene oxide, propylene oxide, butylene oxide or mixtures thereof); amine salts such as amine acetates and diamine salts; quaternary ammonium salts such as quaternary salts, ethoxylated quaternary salts and diquaternary salts; and amine oxides such as alkyldimethylamine oxides and bis-(2-hydroxyethyl)-alkylamine oxides.
  • Also useful for the present compositions are mixtures of nonionic and anionic surfactants or mixtures of nonionic and cationic surfactants. Nonionic, anionic and cationic surfactants and their recommended uses are disclosed in a variety of published references including McCutcheon's Emulsifiers and Detergents, annual American and International Editions published by McCutcheon's Division, The Manufacturing Confectioner Publishing Co.; Sisely and Wood, Encyclopedia of Surface Active Agents, Chemical Publ. Co., Inc., New York, 1964; and A. S. Davidson and B. Milwidsky, Synthetic Detergents, Seventh Edition, John Wiley and Sons, New York, 1987.
  • Compositions of this invention may also contain formulation auxiliaries and additives, known to those skilled in the art as formulation aids (some of which may be considered to also function as solid diluents, liquid diluents or surfactants). Such formulation auxiliaries and additives may control: pH (buffers), foaming during processing (antifoams such polyorganosiloxanes), sedimentation of active ingredients (suspending agents), viscosity (thixotropic thickeners), in-container microbial growth (antimicrobials), product freezing (antifreezes), color (dyes/pigment dispersions), wash-off (film formers or stickers), evaporation (evaporation retardants), and other formulation attributes. Film formers include, for example, polyvinyl acetates, polyvinyl acetate copolymers, polyvinylpyrrolidone-vinyl acetate copolymer, polyvinyl alcohols, polyvinyl alcohol copolymers and waxes. Examples of formulation auxiliaries and additives include those listed in McCutcheon's Volume 2: Functional Materials, annual International and North American editions published by McCutcheon's Division, The Manufacturing Confectioner Publishing Co.; and PCT Publication WO 03/024222.
  • The compounds of Formula 1 and other active ingredients are typically incorporated into the present compositions by dissolving the active ingredient in a solvent or by grinding in a liquid or dry diluent. Solutions, including emulsifiable concentrates, can be prepared by simply mixing the ingredients. If the solvent of a liquid composition intended for use as an emulsifiable concentrate is water-immiscible, an emulsifier is typically added to emulsify the active-containing solvent upon dilution with water. Active ingredient slurries, with particle diameters of up to 2,000 μm can be wet milled using media mills to obtain particles with average diameters below 3 μm. Aqueous slurries can be made into finished suspension concentrates (see, for example, U.S. Pat. No. 3,060,084) or further processed by spray drying to form water-dispersible granules. Dry formulations usually require dry milling processes, which produce average particle diameters in the 2 to 10 μm range. Dusts and powders can be prepared by blending and usually grinding (such as with a hammer mill or fluid-energy mill). Granules and pellets can be prepared by spraying the active material upon preformed granular carriers or by agglomeration techniques. See Browning, “Agglomeration”, Chemical Engineering, Dec. 4, 1967, pp 147-48, Perry's Chemical Engineer's Handbook, 4th Ed., McGraw-Hill, New York, 1963, pages 8-57 and following, and WO 91/13546. Pellets can be prepared as described in U.S. Pat. No. 4,172,714. Water-dispersible and water-soluble granules can be prepared as taught in U.S. Pat. No. 4,144,050, U.S. Pat. No. 3,920,442 and DE 3,246,493. Tablets can be prepared as taught in U.S. Pat. No. 5,180,587, U.S. Pat. No. 5,232,701 and U.S. Pat. No. 5,208,030. Films can be prepared as taught in GB 2,095,558 and U.S. Pat. No. 3,299,566.
  • For further information regarding the art of formulation, see T. S. Woods, “The Formulator's Toolbox—Product Forms for Modern Agriculture” in Pesticide Chemistry and Bioscience, The Food-Environment Challenge, T. Brooks and T. R. Roberts, Eds., Proceedings of the 9th International Congress on Pesticide Chemistry, The Royal Society of Chemistry, Cambridge, 1999, pp. 120-133. See also U.S. Pat. No. 3,235,361, Col. 6, line 16 through Col. 7, line 19 and Examples 10-41; U.S. Pat. No. 3,309,192, Col. 5, line 43 through Col. 7, line 62 and Examples 8, 12, 15, 39, 41, 52, 53, 58, 132, 138-140, 162-164, 166, 167 and 169-182; U.S. Pat. No. 2,891,855, Col. 3, line 66 through Col. 5, line 17 and Examples 1-4; Klingman, Weed Control as a Science, John Wiley and Sons, Inc., New York, 1961, pp 81-96; Hance et al., Weed Control Handbook, 8th Ed., Blackwell Scientific Publications, Oxford, 1989; and Developments in formulation technology, PJB Publications, Richmond, UK, 2000.
  • Without further elaboration, it is believed that one skilled in the art using the preceding formulation description can utilize the present invention to its fullest extent. The following Examples of formulation are, therefore, to be construed as merely illustrative, and not limiting of the disclosure in any way whatsoever. Percentages are by weight, and all formulations are prepared in conventional ways. Compound numbers refer to compounds in Index Table A. The component designations refer to the corresponding compounds indicated in the Component (b) column of Table A1. For example, “Component (b1a)” refers to 1-[4-[4-[5-(2,6-difluorophenyl)-4,5-dihydro-3-isoxazolyl]-2-thiazolyl]-1-piperidinyl]-2-[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]ethanone.
    • Example A
  • High Strength Concentrate
    Any one of Compounds 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 and 12 93.8%
    Component (b1a) 4.7%
    silica aerogel 0.5%
    synthetic amorphous fine silica 1.0%
    • Example B
  • Wettable Powder
    Any one of Compounds 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 and 12 59.1%
    Component (b3a) 5.9%
    dodecylphenol polyethylene glycol ether 2.0%
    sodium ligninsulfonate 4.0%
    sodium silicoaluminate 6.0%
    montmorillonite (calcined) 23.0%
    • Example C
  • Granule
    Any one of Compounds 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 and 12 5.0%
    Component (b4a) 5.0%
    attapulgite granules (low volatile matter, 90.0%
    0.71/0.30 mm; U.S.S. No. 25-50 sieves)
    • Example D
  • Extruded Pellet
    Any one of Compounds 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 and 12 16.7%
    Component (b5) 8.3%
    anhydrous sodium sulfate 10.0%
    crude calcium ligninsulfonate 5.0%
    sodium alkylnaphthalenesulfonate 1.0%
    calcium/magnesium bentonite 59.0%
    • Example E
  • Emulsifiable Concentrate
    Any one of Compounds 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 and 12 6.7%
    Component (b6a) 3.3%
    polyoxyethylene sorbitol hexoleate 20.0%
    C6-C10 fatty acid methyl ester 70.0%
    • Example F
  • Microemulsion
    Any one of Compounds 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 and 12 2.5%
    Component (b7) 2.5%
    polyvinylpyrrolidone-vinyl acetate copolymer 30.0%
    alkylpolyglycoside 30.0%
    glyceryl monooleate 15.0%
    water 20.0%
    • Example G
  • High Strength Concentrate
    Any one of Compounds 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 and 12 49.3%
    Component (b8) 49.2%
    silica aerogel 0.5%
    synthetic amorphous fine silica 1.0%
    • Example H
  • Granule
    Any one of Compounds 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 and 12 5.0%
    Component (b9a) 5.0%
    attapulgite granules (low volatile matter, 90.0%
    0.71/0.30 mm; U.S.S. No. 25-50 sieves)
    • Example I
  • Extruded Pellet
    Any one of Compounds 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 and 12 12.5%
    Component (b10a) 12.5%
    anhydrous sodium sulfate 10.0%
    crude calcium ligninsulfonate 5.0%
    sodium alkylnaphthalenesulfonate 1.0%
    calcium/magnesium bentonite 59.0%
    • Example J
  • Emulsifiable Concentrate
    Any one of Compounds 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 and 12 5.0%
    Component (b11) 5.0%
    polyoxyethylene sorbitol hexoleate 20.0%
    C6-C10 fatty acid methyl ester 70.0%
    • Example K
  • Seed Treatment
    Any one of Compounds 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 and 12 1.05%
    Component (b12) 18.95%
    polyvinylpyrrolidone-vinyl acetate copolymer 5.00%
    montan acid wax 5.00%
    calcium ligninsulfonate 1.00%
    polyoxyethylene/polyoxypropylene block copolymers 1.00%
    stearyl alcohol (POE 20) 2.00%
    polyorganosilane 0.20%
    colorant red dye 0.05%
    water 65.75%
    • Example L
  • Wettable Powder
    Any one of Compounds 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 and 12 41.9%
    Component (b1a) 2.1%
    prothioconazole 21.0%
    dodecylphenol polyethylene glycol ether 2.0%
    sodium ligninsulfonate 4.0%
    sodium silicoaluminate 6.0%
    montmorillonite (calcined) 23.0%
    • Example M
  • Emulsifiable Concentrate
    Any one of Compounds 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 and 12 5.0%
    Component (b13) 5.0%
    polyoxyethylene sorbitol hexoleate 20.0%
    C6-C10 fatty acid methyl ester 70.0%
  • As already mentioned, combinations of components (a), (b) and optionally (c) can be together or separately formulated with at least one of a surfactant, a solid diluent or a liquid diluent. Thus one, two or all three of components (a), (b) and (c) can be formulated together to form a premix composition, or they can be formulated separately and then the formulated compositions combined together before application (e.g., in a spray tank) or, alternatively, applied in succession. In the formulated compositions containing components (a), (b) or (c), the components (a), (b) or (c) are present in biologically effective amounts, or more particularly, for example, fungicidally effective amounts if they are fungicidal or insecticidally effective amounts if they are insecticidal.
  • Formulations are often diluted with water to form aqueous compositions before application. Aqueous compositions for direct applications to the plant or portion thereof (e.g., spray tank compositions) typically comprise at least about 1 ppm or more (e.g., from 1 ppm to 100 ppm) of fungicidally active compounds according to the present invention.
  • The compositions of this invention are useful as plant disease control agents. The present invention therefore further comprises a method for controlling plant diseases caused by fungal plant pathogens comprising applying to the plant or portion thereof to be protected, or to the plant seed or vegetative propagation unit to be protected, an effective amount of a composition of the invention (e.g., a composition comprising component (a), or components (a) and (b), or components (a), (b) and (c)). This aspect of the present invention can also be described as a method for protecting a plant or plant seed from diseases caused by fungal pathogens comprising applying a fungicidally effective amount of a composition of the invention to the plant (or portion thereof) or plant seed (directly or through the environment (e.g., growing medium) of the plant or plant seed).
  • Component (a) compounds and/or combinations thereof with component (b) compounds and/or (c) one or more other biologically active compounds or agents can be applied to plants genetically transformed to express proteins toxic to invertebrate pests (such as Bacillus thuringiensis delta-endotoxins). The effect of the exogenously applied present component (a) alone or in combination with component (b) and optionally component (c) may be synergistic with the expressed toxin proteins.
  • Plant disease control is ordinarily accomplished by applying an effective amount of a composition of the invention (e.g., comprising component (a), or a mixture of components (a), (b) and optionally (c)), typically as a formulated composition, either pre- or post-infection, to the portion of the plant to be protected such as the roots, stems, foliage, fruit, seeds, tubers or bulbs, or to the media (soil or sand) in which the plants to be protected are growing. Component (a) or mixtures thereof can also be applied to seeds to protect the seeds and seedlings developing from the seeds. The mixtures can also be applied through irrigation water to treat plants. Control of postharvest pathogens which infect the produce before harvest is typically accomplished by field application of a composition of the invention, and in cases where infection occurs after harvest the compositions can be applied to the harvested crop as dips, sprays, fumigants, treated wraps or box liners.
  • Suitable rates of application (e.g., fungicidally effective amounts) of component (a) (i.e. at least one compound selected from compounds of Formula 1, N-oxides and salts thereof) as well as suitable rates of application (e.g., biologically effective amounts, fungicidally effective amounts or insecticidally effective amounts) of components (b) and optionally (c) according to this invention can be influenced by many factors of the environment and should be determined under actual use conditions. Foliage can normally be protected when treated at a rate of from less than about 1 g/ha to about 5,000 g/ha of active ingredients. Seed and seedlings can normally be protected when seed is treated at a rate of from about 0.1 to about 10 g per kilogram of seed; and vegetative propagation units (e.g., cuttings and tubers) can normally be protected when propagation unit is treated at a rate of from about 0.1 to about 10 g per kilogram of propagation unit. One skilled in the art can easily determine through simple experimentation the application rates of component (a), and mixtures and compositions thereof, containing particular combinations of active ingredients according to this invention needed to provide the desired spectrum of plant protection and control of plant diseases and optionally other plant pests.
  • The compounds of Formula 1, N-oxides, and salts thereof, are particularly efficacious for controlling plant diseases caused by fungal pathogens, particularly in the Basidomycete and Ascomycete classes. Combining these compounds with other fungicidal compounds can provide control of diseases caused by a broad spectrum of fungal plant pathogens in the Basidiomycete, Ascomycete, Oomycete and Deuteromycete classes. Accordingly, mixtures and compositions described herein can control a broad spectrum of plant diseases, foliar pathogens of crops including: cereal grain crops such as wheat, barley, oats, rye, triticale, rice, maize, sorghum and millet; vine crops such as table and wine grapes; field crops such as oilseed rape (canola), sunflower; sugar beets, sugar cane, soybean, peanuts (groundnut), tobacco, alfalfa, clover, lespedeza, trefoil and vetch; pome fruits such as apple, pear, crabapple, loquat, mayhaw and quince; stone fruits such as peaches, cherries, plums, apricots, nectarines and almonds; citrus fruits such as lemons, limes, oranges, grapefruit, mandarin (tangerines) and kumquat; root and tuber vegetables and field crops (and their foliage) such as artichoke, garden and sugar beet, carrot, cassava, ginger, ginseng, horseradish, parsnip, potato, radish, rutabaga, sweet potato, turnip and yam; bulb vegetables such as garlic, leek, onion and shallot; leafy vegetables such as arugula (roquette), celery, celery, cress, endive (escarole), fennel, head and leaf lettuce, parsley, radicchio (red chicory), rhubarb, spinach and Swiss chard; brassica (cole) leafy vegetables such as broccoli, broccoli raab (rapini), Brussels sprouts, cabbage, bok Choy, cauliflower, collards, kale, kohlrabi, mustard and greens; legume vegetables (succulent or dried) such as lupin, bean (Phaseolus spp.) (including field bean, kidney bean, lima bean, navy bean, pinto bean, runner bean, snap bean, tepary bean and wax bean), bean (Vigna spp.) (including adzuki bean, asparagus bean, blackeyed pea, catjang, Chinese longbean, cowpea, crowder pea, moth bean, mung bean, rice bean, southern pea, urd bean and yardlong bean), broad bean (fava), chickpea (garbanzo), guar, jackbean, lablab bean, lentil and pea (Pisum spp.) (including dwarf pea, edible-podded pea, English pea, field pea, garden pea, green pea, snowpea, sugar snap pea, pigeon pea and soybean); fruiting vegetables such as eggplant, groundcherry (Physalis spp.), pepino and pepper (including bell pepper, chili pepper, cooking pepper, pimento, sweet pepper; tomatillo and tomato); cucurbit vegetables such as Chayote (fruit), Chinese waxgourd (Chinese preserving melon), citron melon, cucumber, gherkin, edible gourd (including hyotan, cucuzza, hechima, and Chinese okra), Momordica spp. (including balsam apple, balsam pear, bittermelon and Chinese cucumber), muskmelon (including cantaloupe and pumpkin), summer and winter squash (including butternut squash, calabaza, hubbard squash, acorn squash, spaghetti squash) and watermelon; berries such as blackberry (including bingleberry, boysenberry, dewberry, lowberry, marionberry, olallieberry and youngberry), blueberry, cranberry, currant, elderberry, gooseberry, huckleberry, loganberry, raspberry and strawberry; tree nuts such as almond, beech nut, Brazil nut, butternut, cashew, chestnut, chinquapin, filbert (hazelnut), hickory nut, macadamia nut, pecan and walnut; tropical fruits and other crops such as bananas, plantains, mangos, coconuts, papaya, guava, avocado, lichee, agave, coffee, cacao, sugar cane, oil palm, sesame, rubber and spices; fiber crops such as cotton, flax and hemp; turfgrasses (including warm- and cool-season turfgrasses) such as bentgrass, Kentucky bluegrass, St. Augustine grass, tall fescue and Bermuda grass.
  • These pathogens include: Oomycetes, including Phytophthora pathogens such as Phytophthora infestans, Phytophthora megasperma, Phytophthora parasitica, Phytophthora cinnamomi and Phytophthora capsici, Pythium pathogens such as Pythium aphanidermatum, and pathogens in the Peronosporaceae family such as Plasmopara viticola, Peronospora spp. (including Peronospora tabacina and Peronospora parasitica), Pseudoperonospora spp. (including Pseudoperonospora cubensis) and Bremia lactucae; Ascomycetes, including Alternaria pathogens such as Alternaria solani and Alternaria brassicae, Guignardia pathogens such as Guignardia bidwelli, Venturia pathogens such as Venturia inaequalis, Septoria pathogens such as Septoria nodorum and Septoria tritici, powdery mildew disease pathogens such as Blumeria spp. (including Blumeria graminis) and Erysiphe spp. (including Erysiphe polygoni), Uncinula necatur, Sphaerotheca fuliginea and Podosphaera leucotricha, Pseudocercosporella herpotrichoides, Botrytis pathogens such as Botrytis cinerea, Monilinia fructicola, Sclerotinia pathogens such as Sclerotinia sclerotiorum and Sclerotinia minor, Magnaporthe grisea, Phomopsis viticola, Helminthosporium pathogens such as Helminthosporium tritici repentis, Pyrenophora teres, anthracnose disease pathogens such as Glomerella or Colletotrichum spp. (such as Colletotrichum graminicola and Colletotrichum orbiculare), and Gaeumannomyces graminis; Basidiomycetes, including rust diseases caused by Puccinia spp. (such as Puccinia recondita, Puccinia striiformis, Puccinia hordei, Puccinia graminis and Puccinia arachidis), Hemileia vastatrix and Phakopsora pachyrhizi; other pathogens including Rhizoctonia spp. (such as Rhizoctonia solani and Rhizoctonia oryzae); Fusarium pathogens such as Fusarium roseum, Fusarium graminearum and Fusarium oxysporum; Verticillium dahliae; Sclerotium rolfsii; Rynchosporium secalis; Cercosporidium personatum, Cercospora arachidicola and Cercospora beticola; Rutstroemia floccosum (also known as Sclerontina homoeocarpa); Rhizopus spp. (such as Rhizopus stolonifer); Aspergillus spp. (such as Aspergillus flavus and Aspergillus parasiticus); and other genera and species closely related to these pathogens. Commonly, pathogens are referred to as diseases, and thus in the preceding sentence the word “pathogen” also refers to the plant disease caused by the pathogen. More precisely, plant diseases are caused by pathogens. Therefore, for example, powdery mildew diseases are plant diseases caused by powdery mildew pathogens, Septoria diseases are plant diseases caused by Septoria pathogens, and rust diseases are plant diseases caused by rust disease pathogens. Certain fungicidal compounds are also bactericidal, and therefore in addition to their fungicidal activity, the compositions or combinations can also have activity against bacteria such as Erwinia amylovora, Xanthomonas campestris, Pseudomonas syringae, and other related species. Furthermore, compounds of Formula 1 and their mixtures and compositions according to this invention are useful in treating postharvest diseases of fruits and vegetables caused by fungi and bacteria. These infections can occur before, during and after harvest. For example, infections can occur before harvest and then remain dormant until some point during ripening (e.g., host begins tissue changes in such a way that infection can progress); also infections can arise from surface wounds created by mechanical or insect injury. In this respect, application of compounds, mixtures and compositions according to this invention can reduce losses (i.e. losses resulting from quantity and quality) due to postharvest diseases which may occur at any time from harvest to consumption. Treatment of postharvest diseases with compounds of the invention can increase the period of time during which perishable edible plant parts (e.g., fruits, seeds, foliage, stems, bulbs, tubers) can be stored refrigerated or unrefrigerated after harvest, and remain edible and free from noticeable or harmful degradation or contamination by fungi or other microorganisms. Treatment of edible plant parts before or after harvest with compounds, mixtures or compositions according to this invention can also decrease the formation of toxic metabolites of fungi or other microorganisms, for example, mycotoxins such as aflatoxins.
  • In the present fungicidal compositions, the Formula 1 compounds of component (a) can work synergically with the additional fungicidal compounds of component (b) to provide such beneficial results as broadening the spectrum of plant diseases controlled, extending duration of preventative and curative protection, and suppressing proliferation of resistant fungal pathogens. In particular embodiments, compositions are provided in accordance with this invention that comprise proportions of component (a) and component (b) that are especially useful for controlling particular fungal diseases (such as Alternaria solani, Blumeria graminis f. sp. tritici, Botrytis cinerea, Puccinia recondita f. sp. tritici, Rhizoctonia solani, Septoria nodorum, Septoria tritici).
  • Mixtures of fungicides may also provide significantly better disease control than could be predicted based on the activity of the individual components. This synergism has been described as “the cooperative action of two components of a mixture, such that the total effect is greater or more prolonged than the sum of the effects of the two (or more) taken independently” (see P. M. L. Tames, Neth. J. Plant Pathology 1964, 70, 73-80). In methods providing plant disease control in which synergy is exhibited from a combination of active ingredients (e.g., fungicidal compounds) applied to the plant or seed, the active ingredients are applied in a synergistic weight ratio and synergistic (i.e. synergistically effective) amounts. Measures of disease control, inhibition and prevention cannot exceed 100%. Therefore expression of substantial synergism typically requires use of application rates of active ingredients wherein the active ingredients separately provide much less than 100% effect, so that their additive effect is substantially less than 100% to allow the possibility of an increase in effect as result of synergism. On the other hand, application rates of active ingredients that are too low may show not show much activity in mixtures even with the benefit of synergism. One skilled in the art can easily identify and optimize through simple experimentation the weight ratios and application rates (i.e. amounts) of fungicidal compounds providing synergy.
  • The following Tests include tests demonstrating the efficacy of compounds of Fomrula 1 for controlling specific pathogens; this efficacy is thus provided to fungicidal mixtures comprising these compounds. The disease control afforded by the present compounds alone or in mixtures is not limited, however, to the pathogenic fungi species exemplified.
  • See Index Table A for compound descriptions. See Index Table B for melting point data. The abbreviation “Cmpd.” stands for “Compound”, and the abbreviation “Ex.” stands for “Example” and is followed by a number indicating in which Synthesis Example the compound is prepared. Mass spectra (M.S.) are reported as the molecular weight of the highest isotopic abundance parent ion (M+1) formed by addition of H+ (molecular weight of 1) to the molecule, observed by mass spectrometry using atmospheric pressure chemical ionization (AP+). The presence of molecular ions containing one or more higher atomic weight isotopes of lower abundance (e.g., 37Cl, 81Br) is not reported.
  •
    INDEX TABLE A
    Figure US20150018374A1-20150115-C00061
    Cmpd No. R1 R2 R3 M.S.
     1 F H Cl 334
     2 F F Cl 352
     3 Cl F Cl *
     4 (Ex. 1) Cl F Br 414
     5 Br F Cl 414
     6 Br H Br 440
     7 Br F Br *
     8 Cl H Br 396
     9 Br H Cl 396
    10 Cl H Cl 350
    11 (Ex. 2) F F Br *
    12 F H Br
    *Melting Point (MP) data are listed in Index Table B.
  • INDEX TABLE B
    Melting Melting
    CmpdNo. Melting Pointa Cmpd No. Point Cmpd No. Point
    3 166-168 7 154-156 11 134-136
    aMelting point data are ° C.
    • Biological Examples of the Invention
  • General protocol for preparing test suspensions for Tests A-I: the test compounds were first dissolved in acetone in an amount equal to 3% of the final volume and then suspended at the desired concentration (in ppm) in acetone and purified water (50/50 mix by volume) containing 250 ppm of the surfactant Trem® 014 (polyhydric alcohol esters). The resulting test suspensions were then used in Tests A-I. Each test was conducted in triplicate, and the results were averaged. Spraying a 200 ppm test suspension to the point of run-off on the test plants was the equivalent of a rate of about 800 g/ha. Unless otherwise indicated, the rating values indicate a 200 ppm test suspension was used. (An asterisk “*” next to the rating value indicates a 40 ppm test suspension was used.)
    • Test A
  • The test suspension was sprayed to the point of run-off on tomato seedlings. The following day the seedlings were inoculated with a spore suspension of Botrytis cinerea (the causal agent of tomato Botrytis) and incubated in saturated atmosphere at 20° C. for 48 h, and then moved to a growth chamber at 24° C. for 3 additional days, after which time visual disease ratings were made.
    • Test B
  • The test suspension was sprayed to the point of run-off on tomato seedlings. The following day the seedlings were inoculated with a spore suspension of Alternaria solani (the causal agent of tomato early blight) and incubated in a saturated atmosphere at 27° C. for 48 h, and then moved to a growth chamber at 20° C. for 5 days, after which time visual disease ratings were made.
    • Test C
  • The test suspension was sprayed to the point of run-off on tomato seedlings. The following day the seedlings were inoculated with a spore suspension of Phytophthora infestans (the causal agent of tomato late blight) and incubated in a saturated atmosphere at 20° C. for 24 h, and then moved to a growth chamber at 20° C. for 5 days, after which time visual disease ratings were made.
    • Test D
  • The test suspension was sprayed to the point of run-off on creeping bent grass (Agrostis sp.) seedlings. The following day the seedlings were inoculated with a bran and mycelial slurry of Rhizoctonia solani (the causal agent of turf brown patch) and incubated in a saturated atmosphere at 27° C. for 48 h, and then moved to a growth chamber at 27° C. for 3 days, after which time disease ratings were made.
    • Test E
  • The test suspension was sprayed to the point of run-off on wheat seedlings. The following day the seedlings were inoculated with a spore suspension of Septoria nodorum (the causal agent of Septoria glume blotch) and incubated in a saturated atmosphere at 24° C. for 48 h, and then moved to a growth chamber at 20° C. for 9 days, after which time visual disease ratings were made.
    • Test F
  • The test suspension was sprayed to the point of run-off on wheat seedlings. The following day the seedlings were inoculated with a spore suspension of Septoria tritici (the causal agent of wheat leaf blotch) and incubated in saturated atmosphere at 24° C. for 48 h. and then the seedlings were moved to a growth chamber at 20° C. for 19 additional days, after which time visual disease ratings were made.
    • Test G
  • Wheat seedlings were inoculated with a spore suspension of Puccinia recondita f. sp. tritici (the causal agent of wheat leaf rust) and incubated in a saturated atmosphere at 20° C. for 24 h, and then moved to a growth chamber at 20° C. for 2 days. At the end of this time the test suspension was sprayed to the point of run-off, and then the seedlings were moved to a growth chamber at 20° C. for 4 days after which time visual disease ratings were made.
    • Test H
  • The test suspension was sprayed to the point of run-off on wheat seedlings. The following day the seedlings were inoculated with a spore suspension of Puccinia recondita f. sp. tritici (the causal agent of wheat leaf rust) and incubated in a saturated atmosphere at 20° C. for 24 h, and then moved to a growth chamber at 20° C. for 6 days, after which time visual disease ratings were made.
    • Test I
  • The test suspension was sprayed to the point of run-off on wheat seedlings. The following day the seedlings were inoculated with a spore dust of Blumeria graminis f. sp. tritici (also known as Erysiphe graminis f. sp. tritici, the causal agent of wheat powdery mildew) and incubated in a growth chamber at 20° C. for 8 days, after which time visual disease ratings were made.
  • Results for Tests A-I are given in Table A. In the Table, a rating of 100 indicates 100% disease control and a rating of 0 indicates no disease control (relative to the controls). A hyphen (-) indicates no test results.
  • TABLE A
    Cmpd Test Test Test Test Test Test Test Test Test
    No. A B C D E F G H I
     1  99  93 0 99  0 100 —  99 100
     2 100 100 — — 87 100  0  99 100
     3 100 100 0* — 99 100 100 100  99
     4 100 — — — — 100 — 100 100
     5 100 — — — — 100 — 100 100
     6  99* — — — — 100* —  96*  99*
     7 100 — — — — 100 — 100 100
     8 100 — — — — 100 —  99 100
     9  99* — — —  0* 100* —  93*  99*
    10 100* — — —  0* 100* —  98* 100*
    11 100* — — — 60* 100* —  98* 100*
    “Cmpd No.” means compound number.
  • The test results presented in Table A for compounds of Formula 1 illustrate the fungicidal activity of component (a) contributing to the plant disease control utility of compositions comprising component (a) in combination with component (b) and optionally component (c) according to the present invention.

Claims (15)

1. A fungicidal composition comprising:
(a) at least one compound selected from the compounds of Formula 1, N-oxides, and salts thereof:
Figure US20150018374A1-20150115-C00062
wherein
R1 is F, Cl or Br;
R2 is H or F; and
R3 is Cl or Br; and
(b) at least one fungicidal compound selected from
Figure US20150018374A1-20150115-C00063
wherein Rb20 and Rb21 are independently CH3, CF2H or CF3; each Rb22 is independently halogen or cyano; n is 0, 1, 2 or 3; and L is a direct bond or —CH2O— wherein the left bond is connected to the dihydroisoxazole ring and the right bond is connected to the phenyl ring;
Figure US20150018374A1-20150115-C00064
wherein Rb1 is
Figure US20150018374A1-20150115-C00065
wherein Rb2 is —CH2OC(O)CH(CH3)2, —C(O)CH3, —CH2OC(O)CH3, —C(O)OCH2CH(CH3)2 or
Figure US20150018374A1-20150115-C00066
wherein Rb3 is CH3 or F;
Figure US20150018374A1-20150115-C00067
wherein Rb4 is —(CH2)4CH3, —C(CH3)3 or —(CH2)2C≡CH;
Figure US20150018374A1-20150115-C00068
wherein Rb5 is H or F, and Rb6 is —CF2CHFCF3 or —CF2CF2H;
Figure US20150018374A1-20150115-C00069
wherein
Rb7 is
Figure US20150018374A1-20150115-C00070
Rb8 is H, halogen or C1-C2 alkyl;
Rb9 is C1-C8 alkyl, C1-C8 haloalkyl or C2-C8 alkoxyalkyl;
Rb10 is halogen, C1-C2 alkyl or C1-C2 haloalkyl;
Rb11 is halogen, C1-C2 alkyl or C1-C2 haloalkyl;
Rb12 is C1-C2 alkyl;
Rb13 is H, halogen or C1-C2 alkyl;
Rb14 is C1-C2 alkyl or C1-C2 haloalkyl;
Rb15 is H, C1-C2 alkyl or C1-C2 haloalkyl;
W is CH or N;
Y is CH or N; and
Z is CH or N;
Figure US20150018374A1-20150115-C00071
and salts thereof.
2. The composition of claim 1 wherein component (a) comprises a compound of Formula 1 or salt thereof.
3. The composition of claim 1 wherein component (a) comprises a compound selected from the group consisting of
4-(2-chloro-4-fluorophenyl)-N-(2-fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine,
4-(2-chloro-4-fluorophenyl)-N-(2-chlorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine,
N-(2-bromophenyl)-4-(2-chloro-4-fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine,
4-(2-bromo-4-fluorophenyl)-N-(2-fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine,
4-(2-bromo-4-fluorophenyl)-N-(2-chlorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine,
4-(2-bromo-4-fluorophenyl)-N-(2-bromophenyl)-1,3-dimethyl-1H-pyrazol-5-amine,
4-(2-chloro-4-fluorophenyl)-N-(2,6-difluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine,
4-(2-chloro-4-fluorophenyl)-N-(2-chloro-6-fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine,
N-(2-bromo-6-fluorophenyl)-4-(2-chloro-4-fluoromethyl)-1,3-dimethyl-1H-pyrazol-5-amine,
4-(2-bromo-4-fluorophenyl)-N-(2,6-difluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine,
4-(2-bromo-4-fluorophenyl)-N-(2-chloro-6-fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine, and
4-(2-bromo-4-fluorophenyl)-N-(2-bromo-6-fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine.
4. The composition of claim 1 further comprising (c) at least one additional compound or agent that is biologically active.
5. The composition of claim 4 wherein component (c) comprises at least one fungicidal compound selected from the group consisting of:
(c1) methyl benzimidazole carbamate fungicides;
(c2) dicarboximide fungicides;
(c3) demethylation inhibitor fungicides;
(c4) phenylamide fungicides;
(c5) amine/morpholine fungicides;
(c6) phospholipid biosynthesis inhibitor fungicides;
(c7) carboxamide fungicides;
(c8) hydroxy(2-amino-)pyrimidine fungicides;
(c9) anilinopyrimidine fungicides;
(c10) N-phenyl carbamate fungicides;
(c11) quinone outside inhibitor fungicides;
(c12) phenylpyrrole fungicides;
(c13) quinoline fungicides;
(c14) lipid peroxidation inhibitor fungicides;
(c15) melanin biosynthesis inhibitors-reductase fungicides;
(c16) melanin biosynthesis inhibitors-dehydratase fungicides;
(c17) hydroxyanilide fungicides;
(c18) squalene-epoxidase inhibitor fungicides;
(c19) polyoxin fungicides;
(c20) phenylurea fungicides;
(c21) quinone inside inhibitor fungicides;
(c22) benzamide fungicides;
(c23) enopyranuronic acid antibiotic fungicides;
(c24) hexopyranosyl antibiotic fungicides;
(c25) glucopyranosyl antibiotic: protein synthesis fungicides;
(c26) glucopyranosyl antibiotic: trehalase and inositol biosynthesis fungicides;
(c27) cyanoacetamideoxime fungicides;
(c28) carbamate fungicides;
(c29) oxidative phosphorylation uncoupling fungicides;
(c30) organo tin fungicides;
(c31) carboxylic acid fungicides;
(c32) heteroaromatic fungicides;
(c33) phosphonate fungicides;
(c34) phthalamic acid fungicides;
(c35) benzotriazine fungicides;
(c36) benzene-sulfonamide fungicides;
(c37) pyridazinone fungicides;
(c38) thiophene-carboxamide fungicides;
(c39) pyrimidinamide fungicides;
(c40) carboxylic acid amide fungicides;
(c41) tetracycline antibiotic fungicides;
(c42) thiocarbamate fungicides;
(c43) benzamide fungicides;
(c44) host plant defense induction fungicides;
(c45) multi-site contact activity fungicides;
(c46) fungicidal compounds other than fungicidal compounds of component (a) and components (c1) through (c45); and salts of compounds of (c1) through (c46).
6. The composition of claim 4 wherein component (c) includes at least one compound selected from acibenzolar-S-methyl, aldimorph, ametoctradin, amisulbrom, anilazine, azaconazole, azoxystrobin, benalaxyl, benalaxyl-M, benodanil, benomyl, benthiavalicarb, benthiavalicarb-isopropyl, bethoxazin, binapacryl, biphenyl, bitertanol, bixafen, blasticidin-S, boscalid, bromuconazole, bupirimate, buthiobate, carboxin, carpropamid, captafol, captan, carbendazim, chloroneb, chlorothalonil, chlozolinate, clotrimazole, copper salts, cyazofamid, cyflufenamid, cymoxanil, cyproconazole, cyprodinil, dichlofluanid, diclocymet, diclomezine, dicloran, diethofencarb, difenoconazole, diflumetorim, dimethirimol, dimethomorph, dimoxystrobin, diniconazole, diniconazole-M, dinocap, dithianon, dodemorph, dodine, edifenphos, enestroburin, epoxiconazole, etaconazole, ethaboxam, ethirimol, etridiazole, famoxadone, fenamidone, fenarimol, fenbuconazole, fenfuram, fenhexamid, fenoxanil, fenpiclonil, fenpropidin, fenpropimorph, fenpyrazamine, fentin acetate, fentin chloride, fentin hydroxide, ferbam, ferimzone, fluazinam, fludioxonil, flumetover, flumorph, fluopicolide, fluopyram, fluoroimide, fluoxastrobin, fluquinconazole, flusilazole, flusulfamide, flutianil, flutolanil, flutriafol, fluxapyroxad, folpet, fosetyl-aluminum, fuberidazole, furalaxyl, furametpyr, hexaconazole, hymexazol, guazatine, imazalil, imibenconazole, iminoctadine, iodocarb, ipconazole, iprobenfos, iprodione, iprovalicarb, isoprothiolane, isopyrazam, isotianil, kasugamycin, kresoxim-methyl, mancozeb, mandipropamid, maneb, mepronil, meptyldinocap, metalaxyl, metalaxyl-M, metconazole, methasulfocarb, metiram, metominostrobin, mepanipyrim, metrafenone, myclobutanil, naftifine, neo-asozin (ferric methanearsonate), nuarimol, octhilinone, ofurace, orysastrobin, oxadixyl, oxolinic acid, oxpoconazole, oxycarboxin, oxytetracycline, penconazole, pencycuron, penflufen, penthiopyrad, pefurazoate, phosphorous acid and salts thereof, phthalide, picoxystrobin, piperalin, polyoxin, probenazole, prochloraz, procymidone, propamocarb, propamocarb-hydrochloride, propiconazole, propineb, proquinazid, prothiocarb, prothioconazole, pyraclostrobin, pyrametostrobin, pyraoxystrobin, pyrazophos, pyribencarb, pyributicarb, pyrifenox, pyrimethanil, pyriofenone, pyroquilon, pyrrolnitrin, quinconazole, quinomethionate, quinoxyfen, quintozene, sedaxane, silthiofam, simeconazole, spiroxamine, streptomycin, sulfur, tebuconazole, tebufloquin, tecloftalam, tecnazene, terbinafine, tetraconazole, thiabendazole, thifluzamide, thiophanate, thiophanate-methyl, thiram, tiadinil, tolclofos-methyl, tolylfluanid, triadimefon, triadimenol, triarimol, triazoxide, tricyclazole, tridemorph, triflumizole, tricyclazole, trifloxystrobin, triforine, trimorphamide, triticonazole, uniconazole, validamycin, valifenalate, vinclozolin, zineb, ziram, zoxamide, N′-[4-[4-chloro-3-(trifluoromethyl)phenoxy]-2,5-dimethylphenyl]-N-ethyl-N-methylmethanimidamide, 5-chloro-6-(2,4,6-trifluorophenyl)-7-(4-methylpiperidin-1-yl)[1,2,4]triazolo[1,5-a]-pyrimidine (BAS600), N-[2-[4-[[3-(4-chlorophenyl)-2-propyn-1-yl]oxy]-3-methoxyphenyl]ethyl]-3-methyl-2-[(methylsulfonyl)amino]butanamide, N-[2-[4-[[3-(4-chlorophenyl)-2-propyn-1-yl]oxy]-3-methoxyphenyl]ethyl]-3-methyl-2-[(ethylsulfonyl)amino]-butanamide, 2-butoxy-6-iodo-3-propyl-4H-1-benzopyran-4-one, 3-[5-(4-chlorophenyl)-2,3-dimethyl-3-isoxazolidinyl]pyridine, 4-fluorophenyl N-[1-[[[1-(4-cyanophenyl)ethyl]-sulfonyl]methyl]propyl]carbamate, N-[[(cyclopropylmethoxy)amino][6-(difluoromethoxy)-2,3-difluorophenyl]methylene]benzeneacetamide, α-(methoxyimino)-N-methyl-2-[[[1-[3-(trifluoromethyl)phenyl]ethoxy]imino]methyl]benzeneacetamide, N-[4-[4-chloro-3-(trifluoromethyl)phenoxy]-2,5-dimethylphenyl]-N-ethyl-N-methylmethanimidamide, N-(4-chloro-2-nitrophenyl)-N-ethyl-4-methylbenzenesulfonamide, 2-[[[[3-(2,6-dichlorophenyl)-1-methyl-2-propen-1-ylidene]amino]oxy]methyl]-α-(methoxyimino)-N-methylbenzeneacetamide, 1-[(2-propenylthio)carbonyl]-2-(1-methylethyl)-4-(2-methylphenyl)-5-amino-1H-pyrazol-3-one, ethyl-6-octyl-[1,2,4]triazolo[1,5-a]pyrimidin-7-ylamine, pentyl N-[4-[[[[(1-methyl-1H-tetrazol-5-yl)phenylmethylene]amino]oxy]methyl]-2-thiazolyl]carbamate, pentyl N-[6-[[[[(1-methyl-1H-tetrazol-5-yl)phenylmethylene]amino]oxy]methyl]-2-pyridinyl]-carbamate, 2-[(3-bromo-6-quinolinyl)oxy]-N-(1,1-dimethyl-2-butyn-1-yl)-2-(methylthio)acetamide, 2-[(3-ethynyl-6-quinolinyl)oxy]-N-[1-(hydroxymethyl)-1-methyl-2-propyn-1-yl]-2-(methylthio)acetamide, N-(1,1-dimethyl-2-butyn-1-yl)-2-[(3-ethynyl-6-quinolinyl)oxy]-2-(methylthio)acetamide and N′-[4-[[3-[(4-chlorophenyl)methyl]-1,2,4-thiadiazol-5-yl]oxy]-2,5-dimethylphenyl]-N-ethyl-N-methylmethanimidamide.
7. A composition comprising the composition of claim 1 and at least one additional component selected from the group consisting of surfactants, solid diluents and liquid diluents.
8. A method for protecting a plant or plant seed from diseases caused by fungal pathogens comprising applying a fungicidally effective amount of the composition of claim 1 to the plant or plant seed.
9. A compound of Formula 14,
Figure US20150018374A1-20150115-C00072
wherein R3 is Cl or Br.
10. A compound of Formula 17,
Figure US20150018374A1-20150115-C00073
wherein
R1 is F, Cl or Br;
R2 is H or F;
R3 is Cl or Br; and
R32 is H, CH3, CH2CH3 or (CH2)2CH3;
provided that when R1 is H, or when R1 and R2 are each F, then R32 is H.
11. The compound of Formula 20,
Figure US20150018374A1-20150115-C00074
wherein R1 is Br and R2 is F.
12. A compound of Formula 22,
Figure US20150018374A1-20150115-C00075
wherein
R1 is F, Cl or Br;
R2 is H or F;
R3 is Cl or Br; and
M is Na or K.
13. The composition of claim 3 further comprising (c) at least one additional compound or agent that is biologically active.
14. The composition of claim 13 wherein component (c) comprises at least one fungicidal compound selected from the group consisting of:
(c1) methyl benzimidazole carbamate fungicides;
(c2) dicarboximide fungicides;
(c3) demethylation inhibitor fungicides;
(c4) phenylamide fungicides;
(c5) amine/morpholine fungicides;
(c6) phospholipid biosynthesis inhibitor fungicides;
(c7) carboxamide fungicides;
(c8) hydroxy(2-amino-)pyrimidine fungicides;
(c9) anilinopyrimidine fungicides;
(c10) N-phenyl carbamate fungicides;
(c11) quinone outside inhibitor fungicides;
(c12) phenylpyrrole fungicides;
(c13) quinoline fungicides;
(c14) lipid peroxidation inhibitor fungicides;
(c15) melanin biosynthesis inhibitors-reductase fungicides;
(c16) melanin biosynthesis inhibitors-dehydratase fungicides;
(c17) hydroxyanilide fungicides;
(c18) squalene-epoxidase inhibitor fungicides;
(c19) polyoxin fungicides;
(c20) phenylurea fungicides;
(c21) quinone inside inhibitor fungicides;
(c22) benzamide fungicides;
(c23) enopyranuronic acid antibiotic fungicides;
(c24) hexopyranosyl antibiotic fungicides;
(c25) glucopyranosyl antibiotic: protein synthesis fungicides;
(c26) glucopyranosyl antibiotic: trehalase and inositol biosynthesis fungicides;
(c27) cyanoacetamideoxime fungicides;
(c28) carbamate fungicides;
(c29) oxidative phosphorylation uncoupling fungicides;
(c30) organo tin fungicides;
(c31) carboxylic acid fungicides;
(c32) heteroaromatic fungicides;
(c33) phosphonate fungicides;
(c34) phthalamic acid fungicides;
(c35) benzotriazine fungicides;
(c36) benzene-sulfonamide fungicides;
(c37) pyridazinone fungicides;
(c38) thiophene-carboxamide fungicides;
(c39) pyrimidinamide fungicides;
(c40) carboxylic acid amide fungicides;
(c41) tetracycline antibiotic fungicides;
(c42) thiocarbamate fungicides;
(c43) benzamide fungicides;
(c44) host plant defense induction fungicides;
(c45) multi-site contact activity fungicides;
(c46) fungicidal compounds other than fungicidal compounds of component (a) and components (c1) through (c45); and salts of compounds of (c1) through (c46).
15. The composition of claim 13 wherein component (c) includes at least one compound selected from acibenzolar-S-methyl, aldimorph, ametoctradin, amisulbrom, anilazine, azaconazole, azoxystrobin, benalaxyl, benalaxyl-M, benodanil, benomyl, benthiavalicarb, benthiavalicarb-isopropyl, bethoxazin, binapacryl, biphenyl, bitertanol, bixafen, blasticidin-S, boscalid, bromuconazole, bupirimate, buthiobate, carboxin, carpropamid, captafol, captan, carbendazim, chloroneb, chlorothalonil, chlozolinate, clotrimazole, copper salts, cyazofamid, cyflufenamid, cymoxanil, cyproconazole, cyprodinil, dichlofluanid, diclocymet, diclomezine, dicloran, diethofencarb, difenoconazole, diflumetorim, dimethirimol, dimethomorph, dimoxystrobin, diniconazole, diniconazole-M, dinocap, dithianon, dodemorph, dodine, edifenphos, enestroburin, epoxiconazole, etaconazole, ethaboxam, ethirimol, etridiazole, famoxadone, fenamidone, fenarimol, fenbuconazole, fenfuram, fenhexamid, fenoxanil, fenpiclonil, fenpropidin, fenpropimorph, fenpyrazamine, fentin acetate, fentin chloride, fentin hydroxide, ferbam, ferimzone, fluazinam, fludioxonil, flumetover, flumorph, fluopicolide, fluopyram, fluoroimide, fluoxastrobin, fluquinconazole, flusilazole, flusulfamide, flutianil, flutolanil, flutriafol, fluxapyroxad, folpet, fosetyl-aluminum, fuberidazole, furalaxyl, furametpyr, hexaconazole, hymexazol, guazatine, imazalil, imibenconazole, iminoctadine, iodocarb, ipconazole, iprobenfos, iprodione, iprovalicarb, isoprothiolane, isopyrazam, isotianil, kasugamycin, kresoxim-methyl, mancozeb, mandipropamid, maneb, mepronil, meptyldinocap, metalaxyl, metalaxyl-M, metconazole, methasulfocarb, metiram, metominostrobin, mepanipyrim, metrafenone, myclobutanil, naftifine, neo-asozin (ferric methanearsonate), nuarimol, octhilinone, ofurace, orysastrobin, oxadixyl, oxolinic acid, oxpoconazole, oxycarboxin, oxytetracycline, penconazole, pencycuron, penflufen, penthiopyrad, pefurazoate, phosphorous acid and salts thereof, phthalide, picoxystrobin, piperalin, polyoxin, probenazole, prochloraz, procymidone, propamocarb, propamocarb-hydrochloride, propiconazole, propineb, proquinazid, prothiocarb, prothioconazole, pyraclostrobin, pyrametostrobin, pyraoxystrobin, pyrazophos, pyribencarb, pyributicarb, pyrifenox, pyrimethanil, pyriofenone, pyroquilon, pyrrolnitrin, quinconazole, quinomethionate, quinoxyfen, quintozene, sedaxane, silthiofam, simeconazole, spiroxamine, streptomycin, sulfur, tebuconazole, tebufloquin, tecloftalam, tecnazene, terbinafine, tetraconazole, thiabendazole, thifluzamide, thiophanate, thiophanate-methyl, thiram, tiadinil, tolclofos-methyl, tolylfluanid, triadimefon, triadimenol, triarimol, triazoxide, tricyclazole, tridemorph, triflumizole, tricyclazole, trifloxystrobin, triforine, trimorphamide, triticonazole, uniconazole, validamycin, valifenalate, vinclozolin, zineb, ziram, zoxamide, N′-[4-[4-chloro-3-(trifluoromethyl)phenoxy]-2,5-dimethylphenyl]-N-ethyl-N-methylmethanimidamide, 5-chloro-6-(2,4,6-trifluorophenyl)-7-(4-methylpiperidin-1-yl)[1,2,4]triazolo[1,5-a]-pyrimidine (BAS600), N-[2-[4-[[3-(4-chlorophenyl)-2-propyn-1-yl]oxy]-3-methoxyphenyl]ethyl]-3-methyl-2-[(methylsulfonyl)amino]butanamide, N-[2-[4-[[3-(4-chlorophenyl)-2-propyn-1-yl]oxy]-3-methoxyphenyl]ethyl]-3-methyl-2-[(ethylsulfonyl)amino]-butanamide, 2-butoxy-6-iodo-3-propyl-4H-1-benzopyran-4-one, 3-[5-(4-chlorophenyl)-2,3-dimethyl-3-isoxazolidinyl]pyridine, 4-fluorophenyl N-[1-[[[1-(4-cyanophenyl)ethyl]-sulfonyl]methyl]propyl]carbamate, N-[[(cyclopropylmethoxy)amino][6-(difluoromethoxy)-2,3-difluorophenyl]methylene]benzeneacetamide, α-(methoxyimino)-N-methyl-2-[[[1-[3-(trifluoromethyl)phenyl]ethoxy]imino]methyl]benzeneacetamide, N-[4-[4-chloro-3-(trifluoromethyl)phenoxy]-2,5-dimethylphenyl]-N-ethyl-N-methylmethanimidamide, N-(4-chloro-2-nitrophenyl)-N-ethyl-4-methylbenzenesulfonamide, 2-[[[[3-(2,6-dichlorophenyl)-1-methyl-2-propen-1-ylidene]amino]oxy]methyl]-α-(methoxyimino)-N-methylbenzeneacetamide, 1-[(2-propenylthio)carbonyl]-2-(1-methylethyl)-4-(2-methylphenyl)-5-amino-1H-pyrazol-3-one, ethyl-6-octyl-[1,2,4]triazolo[1,5-a]pyrimidin-7-ylamine, pentyl N-[4-[[[[(1-methyl-1H-tetrazol-5-yl)phenylmethylene]amino]oxy]methyl]-2-thiazolyl]carbamate, pentyl N-[6-[[[[(1-methyl-1H-tetrazol-5-yl)phenylmethylene]amino]oxy]methyl]-2-pyridinyl]-carbamate, 2-[(3-bromo-6-quinolinyl)oxy]-N-(1,1-dimethyl-2-butyn-1-yl)-2-(methylthio)acetamide, 2-[(3-ethynyl-6-quinolinyl)oxy]-N-[1-(hydroxymethyl)-1-methyl-2-propyn-1-yl]-2-(methylthio)acetamide, N-(1,1-dimethyl-2-butyn-1-yl)-2-[(3-ethynyl-6-quinolinyl)oxy]-2-(methylthio)acetamide and N′-[4-[[3-[(4-chlorophenyl)methyl]-1,2,4-thiadiazol-5-yl]oxy]-2,5-dimethylphenyl]-N-ethyl-N-methylmethanimidamide.
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Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9107412B2 (en) 2010-09-01 2015-08-18 E I Du Pont De Nemours And Company Fungicidal pyrazoles and their mixtures
US20160075661A1 (en) * 2013-05-20 2016-03-17 E.I. Du Pont De Nemours And Company Solid forms of fungicidal pyrazoles
US10173971B2 (en) 2014-12-30 2019-01-08 Dow Agrosciences Llc Picolinamides with fungicidal activity
US10172358B2 (en) 2016-08-30 2019-01-08 Dow Agrosciences Llc Thiopicolinamide compounds with fungicidal activity
US10173982B2 (en) 2016-08-30 2019-01-08 Dow Agrosciences Llc Picolinamides as fungicides
US10173981B2 (en) 2014-12-30 2019-01-08 Dow Agrosciences Llc Picolinamides as fungicides
US10188109B2 (en) 2014-12-30 2019-01-29 Dow Agrosciences Llc Picolinamide compounds with fungicidal activity
US10244754B2 (en) 2016-08-30 2019-04-02 Dow Agrosciences Llc Picolinamide N-oxide compounds with fungicidal activity
US10246417B2 (en) 2017-01-05 2019-04-02 Dow Agrosciences Llc Picolinamides as fungicides
US10334852B2 (en) 2016-08-30 2019-07-02 Dow Agrosciences Llc Pyrido-1,3-oxazine-2,4-dione compounds with fungicidal activity
US10433555B2 (en) 2014-12-30 2019-10-08 Dow Agrosciences Llc Picolinamide compounds with fungicidal activity
US12114660B2 (en) 2014-12-30 2024-10-15 Corteva Agriscience Llc Picolinamide compounds with fungicidal activity

Families Citing this family (196)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TR201908611T4 (en) 2009-10-07 2019-07-22 Dow Agrosciences Llc Synergistic fungicidal mixtures containing epoxiconazole for fighting fungus in cereals.
KR20150013690A (en) * 2012-05-07 2015-02-05 다우 아그로사이언시즈 엘엘씨 Macrocycle picolinamides as fungicides
AU2013370491B2 (en) 2012-12-28 2016-10-06 Corteva Agriscience Llc Synergistic fungicidal mixtures for fungal control in cereals
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WO2014130241A1 (en) * 2013-02-20 2014-08-28 E. I. Du Pont De Nemours And Company Fungicidal pyrazoles
AR097314A1 (en) * 2013-07-10 2016-03-09 Meiji Seika Pharma Co Ltd SYNERGIC COMPOSITIONS FOR THE CONTROL OF DISEASES IN PLANTS, WHICH INCLUDE DERIVATIVES OF PICOLINIC ACID
CN105658061B (en) * 2013-10-16 2018-06-22 拜耳作物科学股份公司 Active agent combinations comprising (thio) carboxamide derivative and Fungicidal compounds
WO2015100184A1 (en) 2013-12-26 2015-07-02 Dow Agrosciences Llc Use of macrocyclic picolinamides as fungicides
CN106061257A (en) 2013-12-26 2016-10-26 美国陶氏益农公司 Use of macrocyclic picolinamides as fungicides
AU2014373921B2 (en) * 2013-12-31 2017-08-31 Corteva Agriscience Llc Synergistic fungicidal mixtures for fungal control in cereals
JP2015147743A (en) * 2014-02-06 2015-08-20 住友化学株式会社 Plant disease control composition and plant disease control method
US9700047B2 (en) 2014-05-06 2017-07-11 Dow Agrosciences Llc Macrocyclic picolinamides as fungicides
EP3140289A1 (en) 2014-05-06 2017-03-15 E. I. du Pont de Nemours and Company Fungicidal pyrazoles
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CN106470983A (en) 2014-07-08 2017-03-01 美国陶氏益农公司 Big ring picolinamide as antifungal
US9955691B2 (en) 2014-07-08 2018-05-01 Dow Agrosciences Llc Macrocyclic picolinamides as fungicides
WO2016012424A1 (en) 2014-07-24 2016-01-28 Bayer Cropscience Aktiengesellschaft Fungicidal pyrazole derivatives
WO2016024350A1 (en) 2014-08-13 2016-02-18 株式会社エス・ディー・エス バイオテック Condensed 11-membered ring compounds and agricultural and horticultural fungicide containing same
WO2016060230A1 (en) * 2014-10-16 2016-04-21 日本農薬株式会社 Horticultural fungicide and method of using same
WO2016071167A1 (en) * 2014-11-07 2016-05-12 Basf Se Pesticidal mixtures
LT3240414T (en) * 2014-12-30 2022-09-26 Corteva Agriscience Llc Fungicidal compositions
WO2016149311A1 (en) 2015-03-19 2016-09-22 E I Du Pont De Nemours And Company Fungicidal pyrazoles
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EP3512337A1 (en) 2016-09-13 2019-07-24 Basf Se Fungicidal mixtures i comprising quinoline fungicides
WO2018052838A1 (en) 2016-09-16 2018-03-22 E. I. Du Pont De Nemours And Company Fungicidal pyrazoles
WO2018054711A1 (en) 2016-09-26 2018-03-29 Basf Se Pyridine compounds for controlling phytopathogenic harmful fungi
WO2018054721A1 (en) 2016-09-26 2018-03-29 Basf Se Pyridine compounds for controlling phytopathogenic harmful fungi
WO2018054723A1 (en) 2016-09-26 2018-03-29 Basf Se Pyridine compounds for controlling phytopathogenic harmful fungi
WO2018065182A1 (en) 2016-10-04 2018-04-12 Basf Se Reduced quinoline compounds as antifuni agents
WO2018073110A1 (en) 2016-10-20 2018-04-26 Basf Se Quinoline compounds as fungicides
WO2018114393A1 (en) 2016-12-19 2018-06-28 Basf Se Substituted oxadiazoles for combating phytopathogenic fungi
EP3339297A1 (en) 2016-12-20 2018-06-27 Basf Se Substituted oxadiazoles for combating phytopathogenic fungi
EP3338552A1 (en) 2016-12-21 2018-06-27 Basf Se Use of a tetrazolinone fungicide on transgenic plants
US20190359589A1 (en) 2017-01-23 2019-11-28 Basf Se Fungicidal pyridine compounds
WO2018149754A1 (en) 2017-02-16 2018-08-23 Basf Se Pyridine compounds
EP3585773B1 (en) 2017-02-21 2021-04-07 Basf Se Substituted oxadiazoles for combating phytopathogenic fungi
AU2018241628B2 (en) 2017-03-31 2022-03-17 Basf Se Pyrimidinium compounds and their mixtures for combating animal pests
BR112019020879A2 (en) 2017-04-06 2020-04-28 Basf Se compounds, composition, use of a compound of formula i, method to combat phytopathogenic fungi, seed and intermediates
WO2018184970A1 (en) 2017-04-07 2018-10-11 Basf Se Substituted oxadiazoles for combating phytopathogenic fungi
WO2018188962A1 (en) 2017-04-11 2018-10-18 Basf Se Substituted oxadiazoles for combating phytopathogenic fungi
TW201838965A (en) 2017-04-20 2018-11-01 印度商Ｐｉ工業公司 Novel phenylamine compounds
KR102659552B1 (en) 2017-05-02 2024-04-23 코르테바 애그리사이언스 엘엘씨 Use of acyclic picolinamide compounds as fungicides against fungal diseases on turf grasses
EP3618629A1 (en) 2017-05-02 2020-03-11 Basf Se Fungicidal mixture comprising substituted 3-phenyl-5-(trifluoromethyl)-1,2,4-oxadiazoles
TW201842851A (en) 2017-05-02 2018-12-16 美商陶氏農業科學公司 Synergistic mixtures for fungal control in cereals
TWI774761B (en) 2017-05-02 2022-08-21 美商科迪華農業科技有限責任公司 Synergistic mixtures for fungal control in cereals
WO2018202491A1 (en) 2017-05-04 2018-11-08 Basf Se Substituted trifluoromethyloxadiazoles for combating phytopathogenic fungi
US20210084900A1 (en) 2017-05-04 2021-03-25 Basf Se Substituted 5-(haloalkyl)-5-hydroxy-isoxazoles for Combating Phytopathogenic Fungi
BR112019022206A2 (en) 2017-05-05 2020-05-12 Basf Se FUNGICIDAL MIXTURES, AGRICULTURAL COMPOSITION, USE OF THE MIXTURE, METHODS FOR CONTROLLING PHYTOPATHOGENIC HARMFUL FUNGI AND PROTECTION OF PLANT PROPAGATION MATERIAL AND PLANT PROPAGATION MATERIAL
WO2018210661A1 (en) 2017-05-15 2018-11-22 Basf Se Heteroaryl compounds as agrochemical fungicides
WO2018210660A1 (en) 2017-05-15 2018-11-22 Basf Se Heteroaryl compounds as agrochemical fungicides
WO2018210658A1 (en) 2017-05-15 2018-11-22 Basf Se Heteroaryl compounds as agrochemical fungicides
WO2018210659A1 (en) 2017-05-15 2018-11-22 Basf Se Heteroaryl compounds as agrochemical fungicides
AR111804A1 (en) * 2017-05-19 2019-08-21 Sumitomo Chemical Co METHOD FOR CONTROLLING A MULTIPHARM RESISTANT PHYTO-DISEASE OF EFLUJO TYPE
US11737463B2 (en) 2017-05-30 2023-08-29 Basf Se Pyridine and pyrazine compounds
WO2018219797A1 (en) 2017-06-02 2018-12-06 Basf Se Substituted oxadiazoles for combating phytopathogenic fungi
EP3642187A1 (en) 2017-06-19 2020-04-29 Basf Se 2-[[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]aryloxy](thio)acetamides for combating phytopathogenic fungi
WO2019002158A1 (en) 2017-06-30 2019-01-03 Basf Se Substituted trifluoromethyloxadiazoles for combating phytopathogenic fungi
US11477984B2 (en) 2017-07-05 2022-10-25 BASF Agro B.V. Fungicidal mixtures of mefentrifluconazole
WO2019007719A1 (en) 2017-07-07 2019-01-10 Basf Se Pesticidal mixtures
EP3427587A1 (en) 2017-07-10 2019-01-16 Basf Se Pesticidal mixtures
WO2019025250A1 (en) 2017-08-04 2019-02-07 Basf Se Substituted trifluoromethyloxadiazoles for combating phytopathogenic fungi
WO2019038042A1 (en) 2017-08-21 2019-02-28 Basf Se Substituted trifluoromethyloxadiazoles for combating phytopathogenic fungi
WO2019042800A1 (en) 2017-08-29 2019-03-07 Basf Se Pesticidal mixtures
WO2019042932A1 (en) 2017-08-31 2019-03-07 Basf Se Method of controlling rice pests in rice
EP3453706A1 (en) 2017-09-08 2019-03-13 Basf Se Pesticidal imidazole compounds
WO2019052932A1 (en) 2017-09-18 2019-03-21 Basf Se Substituted trifluoromethyloxadiazoles for combating phytopathogenic fungi
WO2019057660A1 (en) 2017-09-25 2019-03-28 Basf Se Indole and azaindole compounds with substituted 6-membered aryl and heteroaryl rings as agrochemical fungicides
CN111201227B (en) 2017-10-13 2024-03-15 巴斯夫欧洲公司 Imidazolium compounds for combating animal pests
US11147275B2 (en) 2017-11-23 2021-10-19 Basf Se Substituted trifluoromethyloxadiazoles for combating phytopathogenic fungi
WO2019115511A1 (en) 2017-12-14 2019-06-20 Basf Se Fungicidal mixture comprising substituted 3-phenyl-5-(trifluoromethyl)-1,2,4-oxadiazoles
WO2019115343A1 (en) 2017-12-15 2019-06-20 Basf Se Fungicidal mixture comprising substituted pyridines
WO2019121143A1 (en) 2017-12-20 2019-06-27 Basf Se Substituted cyclopropyl derivatives
CA3085651A1 (en) 2017-12-20 2019-06-27 Pi Industries Ltd. Fluoralkenyl compounds, process for preparation and use thereof
CA3087313A1 (en) 2018-01-09 2019-08-01 Basf Se Silylethynyl hetaryl compounds as nitrification inhibitors
WO2019137995A1 (en) 2018-01-11 2019-07-18 Basf Se Novel pyridazine compounds for controlling invertebrate pests
WO2019150311A1 (en) 2018-02-02 2019-08-08 Pi Industries Ltd. 1-3 dithiol compounds and their use for the protection of crops from phytopathogenic microorganisms
BR112020014817A2 (en) 2018-02-07 2020-12-08 Basf Se USE OF COMPOUNDS OF FORMULA I, COMPOUNDS OF FORMULA I, COMPOSITION, USE OF A COMPOUND OF FORMULA I, METHOD FOR COMBATING PHYTOPATHOGENIC FUNGI AND SEED
WO2019154665A1 (en) 2018-02-07 2019-08-15 Basf Se New pyridine carboxamides
EP3530118A1 (en) 2018-02-26 2019-08-28 Basf Se Fungicidal mixtures
EP3530116A1 (en) 2018-02-27 2019-08-28 Basf Se Fungicidal mixtures comprising xemium
CN111683528B (en) 2018-02-28 2022-12-13 巴斯夫欧洲公司 Use of pyrazolidinopropyl ethers as nitrification inhibitors
WO2019166252A1 (en) 2018-02-28 2019-09-06 Basf Se Fungicidal mixtures comprising fenpropidin
US12075780B2 (en) 2018-02-28 2024-09-03 Basf Se Use of alkoxypyrazoles as nitrification inhibitors
IL302719A (en) 2018-02-28 2023-07-01 Basf Se Use of n-functionalized alkoxy pyrazole compounds as nitrification inhibitors
WO2019166257A1 (en) 2018-03-01 2019-09-06 BASF Agro B.V. Fungicidal compositions of mefentrifluconazole
EP3533333A1 (en) 2018-03-02 2019-09-04 Basf Se Fungicidal mixtures comprising pydiflumetofen
EP3533331A1 (en) 2018-03-02 2019-09-04 Basf Se Fungicidal mixtures comprising pydiflumetofen
EP3536150A1 (en) 2018-03-06 2019-09-11 Basf Se Fungicidal mixtures comprising fluxapyroxad
BR102019004480B1 (en) 2018-03-08 2023-03-28 Dow Agrosciences Llc PICOLINAMIDES AS FUNGICIDES
WO2019175712A1 (en) 2018-03-14 2019-09-19 Basf Corporation New uses for catechol molecules as inhibitors to glutathione s-transferase metabolic pathways
WO2019175713A1 (en) 2018-03-14 2019-09-19 Basf Corporation New catechol molecules and their use as inhibitors to p450 related metabolic pathways
CN108383791A (en) * 2018-04-27 2018-08-10 上海泰禾国际贸易有限公司 A kind of amides compound and its preparation method and application
WO2019219464A1 (en) 2018-05-15 2019-11-21 Basf Se Substituted trifluoromethyloxadiazoles for combating phytopathogenic fungi
JP7433244B2 (en) 2018-05-15 2024-02-19 ビーエーエスエフ ソシエタス・ヨーロピア Mixtures containing benzpyrimoxane and oxazosulfil and methods of use and application thereof
WO2019224092A1 (en) 2018-05-22 2019-11-28 Basf Se Pesticidally active c15-derivatives of ginkgolides
WO2020002472A1 (en) 2018-06-28 2020-01-02 Basf Se Use of alkynylthiophenes as nitrification inhibitors
MX2021000491A (en) * 2018-07-14 2021-04-12 Fmc Corp Pesticidal mixtures comprising indazoles.
EP3826983B1 (en) 2018-07-23 2024-05-15 Basf Se Use of substituted 2-thiazolines as nitrification inhibitors
EP3826982B1 (en) 2018-07-23 2023-11-01 Basf Se Use of a substituted thiazolidine compound as nitrification inhibitor
WO2020035826A1 (en) 2018-08-17 2020-02-20 Pi Industries Ltd. 1,2-dithiolone compounds and use thereof
EP3613736A1 (en) 2018-08-22 2020-02-26 Basf Se Substituted glutarimide derivatives
TW202400547A (en) * 2018-09-06 2024-01-01 美商富曼西公司 Fungicidal nitroanilino substituted pyrazoles
EP3628157A1 (en) 2018-09-28 2020-04-01 Basf Se Method of controlling insecticide resistant insects and virus transmission to plants
EP3628156A1 (en) 2018-09-28 2020-04-01 Basf Se Method for controlling pests of sugarcane, citrus, rapeseed, and potato plants
EP3628158A1 (en) 2018-09-28 2020-04-01 Basf Se Pesticidal mixture comprising a mesoionic compound and a biopesticide
WO2020064492A1 (en) 2018-09-28 2020-04-02 Basf Se Method of controlling pests by seed treatment application of a mesoionic compound or mixture thereof
WO2020081382A1 (en) 2018-10-15 2020-04-23 Dow Agrosciences Llc Methods for sythesis of oxypicolinamides
EP3643705A1 (en) 2018-10-24 2020-04-29 Basf Se Pesticidal compounds
WO2020095161A1 (en) 2018-11-05 2020-05-14 Pi Industries Ltd. Nitrone compounds and use thereof
EP3670501A1 (en) 2018-12-17 2020-06-24 Basf Se Substituted [1,2,4]triazole compounds as fungicides
EP3696177A1 (en) 2019-02-12 2020-08-19 Basf Se Heterocyclic compounds for the control of invertebrate pests
CN113453555B (en) 2019-02-20 2023-08-08 巴斯夫欧洲公司 Pesticidal mixtures comprising pyrazole compounds
EP3730489A1 (en) 2019-04-25 2020-10-28 Basf Se Heteroaryl compounds as agrochemical fungicides
EP3769623A1 (en) 2019-07-22 2021-01-27 Basf Se Mesoionic imidazolium compounds and derivatives for combating animal pests
BR112021019416A2 (en) 2019-05-29 2021-12-07 Basf Se Compounds, composition, methods of protecting crops and combating, controlling, preventing or protecting against infestations, non-therapeutic method of treating infested animals, seed and use
BR112021021028A2 (en) 2019-06-06 2021-12-14 Basf Se Use of compounds of formula i, compounds of formula i, composition and method to combat phytopathogenic fungi
WO2020244970A1 (en) 2019-06-06 2020-12-10 Basf Se New carbocyclic pyridine carboxamides
WO2020244969A1 (en) 2019-06-06 2020-12-10 Basf Se Pyridine derivatives and their use as fungicides
EP3766879A1 (en) 2019-07-19 2021-01-20 Basf Se Pesticidal pyrazole derivatives
WO2021063736A1 (en) 2019-10-02 2021-04-08 Basf Se Bicyclic pyridine derivatives
WO2021063735A1 (en) 2019-10-02 2021-04-08 Basf Se New bicyclic pyridine derivatives
US20230039941A1 (en) 2019-12-23 2023-02-09 Basf Se Enzyme enhanced root uptake of agrochemical active compound
US20230106291A1 (en) 2020-02-28 2023-04-06 BASF Agro B.V. Methods and uses of a mixture comprising alpha-cypermethrin and dinotefuran for controlling invertebrate pests in t
EP4114185A1 (en) 2020-03-04 2023-01-11 Basf Se Use of substituted 1,2,4-oxadiazoles for combating phytopathogenic fungi
TW202200012A (en) 2020-03-11 2022-01-01 美商富曼西公司 Fungicidal mixtures
BR112022020612A2 (en) 2020-04-14 2022-11-29 Basf Se FUNGICIDAL MIXTURE, AGROCHEMICAL COMPOSITION, NON-THERAPEUTIC USE OF THE MIXTURE AND METHOD TO CONTROL HARMFUL PHYTOPATHOGENIC FUNGI
WO2021219513A1 (en) 2020-04-28 2021-11-04 Basf Se Pesticidal compounds
EP3903584A1 (en) 2020-04-28 2021-11-03 Basf Se Use of strobilurin type compounds for combating phytopathogenic fungi containing an amino acid substitution f129l in the mitochondrial cytochrome b protein conferring resistance to qo inhibitors iv
EP3903582A1 (en) 2020-04-28 2021-11-03 Basf Se Use of strobilurin type compounds for combating phytopathogenic fungi containing an amino acid substitution f129l in the mitochondrial cytochrome b protein conferring resistance to qo inhibitors ii
EP3903581A1 (en) 2020-04-28 2021-11-03 Basf Se Use of strobilurin type compounds for combating phytopathogenic fungi containing an amino acid substitution f129l in the mitochondrial cytochrome b protein conferring resistance to qo inhibitors i
EP3903583A1 (en) 2020-04-28 2021-11-03 Basf Se Use of strobilurin type compounds for combating phytopathogenic fungi containing an amino acid substitution f129l in the mitochondrial cytochrome b protein conferring resistance to qo inhibitors iii
EP3909950A1 (en) 2020-05-13 2021-11-17 Basf Se Heterocyclic compounds for the control of invertebrate pests
EP3945089A1 (en) 2020-07-31 2022-02-02 Basf Se Use of strobilurin type compounds for combating phytopathogenic fungi containing an amino acid substitution f129l in the mitochondrial cytochrome b protein conferring resistance to qo inhibitors v
WO2021249800A1 (en) 2020-06-10 2021-12-16 Basf Se Substituted [1,2,4]triazole compounds as fungicides
EP3960727A1 (en) 2020-08-28 2022-03-02 Basf Se Use of strobilurin type compounds for combating phytopathogenic fungi containing an amino acid substitution f129l in the mitochondrial cytochrome b protein conferring resistance to qo inhibitors vi
EP3939961A1 (en) 2020-07-16 2022-01-19 Basf Se Strobilurin type compounds and their use for combating phytopathogenic fungi
WO2022017836A1 (en) 2020-07-20 2022-01-27 BASF Agro B.V. Fungicidal compositions comprising (r)-2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-1- (1,2,4-triazol-1-yl)propan-2-ol
EP3970494A1 (en) 2020-09-21 2022-03-23 Basf Se Use of strobilurin type compounds for combating phytopathogenic fungi containing an amino acid substitution f129l in the mitochondrial cytochrome b protein conferring resistance to qo inhibitors viii
AR123594A1 (en) 2020-09-26 2022-12-21 Pi Industries Ltd NEMATICIDAL COMPOUNDS AND THEIR USE
WO2022089969A1 (en) 2020-10-27 2022-05-05 BASF Agro B.V. Compositions comprising mefentrifluconazole
WO2022090071A1 (en) 2020-11-02 2022-05-05 Basf Se Use of mefenpyr-diethyl for controlling phytopathogenic fungi
WO2022090069A1 (en) 2020-11-02 2022-05-05 Basf Se Compositions comprising mefenpyr-diethyl
WO2022106304A1 (en) 2020-11-23 2022-05-27 BASF Agro B.V. Compositions comprising mefentrifluconazole
EP4018830A1 (en) 2020-12-23 2022-06-29 Basf Se Pesticidal mixtures
CA3206495A1 (en) 2021-02-02 2022-08-11 Alexander Wissemeier Synergistic action of dcd and alkoxypyrazoles as nitrification inhibitors
EP4043444A1 (en) 2021-02-11 2022-08-17 Basf Se Substituted isoxazoline derivatives
WO2022238157A1 (en) 2021-05-11 2022-11-17 Basf Se Fungicidal mixtures comprising substituted 3-phenyl-5-(trifluoromethyl)-1,2,4-oxadiazoles
JP2024519813A (en) 2021-05-18 2024-05-21 ビーエーエスエフ ソシエタス・ヨーロピア New substituted pyridines as fungicides.
AU2022279357A1 (en) 2021-05-18 2023-11-30 Basf Se New substituted pyridines as fungicides
US20240270728A1 (en) 2021-05-18 2024-08-15 Basf Se New substituted quinolines as fungicides
CA3219128A1 (en) 2021-05-21 2022-11-24 Barbara Nave Use of an n-functionalized alkoxy pyrazole compound as nitrification inhibitor
CA3219022A1 (en) 2021-05-21 2022-11-24 Barbara Nave Use of ethynylpyridine compounds as nitrification inhibitors
EP4094579A1 (en) 2021-05-28 2022-11-30 Basf Se Pesticidal mixtures comprising metyltetraprole
EP4358725A1 (en) 2021-06-21 2024-05-01 Basf Se Metal-organic frameworks with pyrazole-based building blocks
EP4119547A1 (en) 2021-07-12 2023-01-18 Basf Se Triazole compounds for the control of invertebrate pests
KR20240042636A (en) 2021-08-02 2024-04-02 바스프 에스이 (3-pyridyl)-quinazoline
JP2024528936A (en) 2021-08-02 2024-08-01 ビーエーエスエフ ソシエタス・ヨーロピア (3-Quinolyl)-quinazoline
EP4140986A1 (en) 2021-08-23 2023-03-01 Basf Se Pyrazine compounds for the control of invertebrate pests
EP4140995A1 (en) 2021-08-27 2023-03-01 Basf Se Pyrazine compounds for the control of invertebrate pests
EP4151631A1 (en) 2021-09-20 2023-03-22 Basf Se Heterocyclic compounds for the control of invertebrate pests
WO2023072670A1 (en) 2021-10-28 2023-05-04 Basf Se Use of strobilurin type compounds for combating phytopathogenic fungi containing an amino acid substitution f129l in the mitochondrial cytochrome b protein conferring resistance to qo inhibitors x
WO2023072671A1 (en) 2021-10-28 2023-05-04 Basf Se Use of strobilurin type compounds for combating phytopathogenic fungi containing an amino acid substitution f129l in the mitochondrial cytochrome b protein conferring resistance to qo inhibitors ix
EP4194453A1 (en) 2021-12-08 2023-06-14 Basf Se Pyrazine compounds for the control of invertebrate pests
EP4198033A1 (en) 2021-12-14 2023-06-21 Basf Se Heterocyclic compounds for the control of invertebrate pests
EP4198023A1 (en) 2021-12-16 2023-06-21 Basf Se Pesticidally active thiosemicarbazone compounds
EP4238971A1 (en) 2022-03-02 2023-09-06 Basf Se Substituted isoxazoline derivatives
WO2023203066A1 (en) 2022-04-21 2023-10-26 Basf Se Synergistic action as nitrification inhibitors of dcd oligomers with alkoxypyrazole and its oligomers
WO2024028243A1 (en) 2022-08-02 2024-02-08 Basf Se Pyrazolo pesticidal compounds
EP4342885A1 (en) 2022-09-20 2024-03-27 Basf Se N-(3-(aminomethyl)-phenyl)-5-(4-phenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazol-3-amine derivatives and similar compounds as pesticides
EP4361126A1 (en) 2022-10-24 2024-05-01 Basf Se Use of strobilurin type compounds for combating phytopathogenic fungi containing an amino acid substitution f129l in the mitochondrial cytochrome b protein conferring resistance to qo inhibitors xv
WO2024104813A1 (en) 2022-11-14 2024-05-23 Basf Se Fungicidal mixture comprising substituted pyridines
WO2024104815A1 (en) 2022-11-16 2024-05-23 Basf Se Substituted benzodiazepines as fungicides
WO2024104822A1 (en) 2022-11-16 2024-05-23 Basf Se Substituted tetrahydrobenzodiazepine as fungicides
WO2024104814A1 (en) 2022-11-16 2024-05-23 Basf Se Fungicidal mixture comprising substituted pyridines
WO2024104823A1 (en) 2022-11-16 2024-05-23 Basf Se New substituted tetrahydrobenzoxazepine
WO2024104818A1 (en) 2022-11-16 2024-05-23 Basf Se Substituted benzodiazepines as fungicides
EP4389210A1 (en) 2022-12-21 2024-06-26 Basf Se Heteroaryl compounds for the control of invertebrate pests
WO2024165343A1 (en) 2023-02-08 2024-08-15 Basf Se New substituted quinoline compounds for combatitng phytopathogenic fungi
WO2024194038A1 (en) 2023-03-17 2024-09-26 Basf Se Substituted pyridyl/pyrazidyl dihydrobenzothiazepine compounds for combatting phytopathogenic fungi
EP4455137A1 (en) 2023-04-24 2024-10-30 Basf Se Pyrimidine compounds for the control of invertebrate pests
WO2024223034A1 (en) 2023-04-26 2024-10-31 Basf Se Use of strobilurin type compounds for combating phytopathogenic fungi containing an amino acid substitution f129l in the mitochondrial cytochrome b protein conferring resistance to qo inhibitors xvi

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2010123791A1 (en) * 2009-04-22 2010-10-28 E. I. Du Pont De Nemours And Company Solid forms of an azocyclic amide
WO2012031061A2 (en) * 2010-09-01 2012-03-08 E. I. Du Pont De Nemours And Company Fungicidal pyrazoles and their mixtures

Family Cites Families (57)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2891855A (en) 1954-08-16 1959-06-23 Geigy Ag J R Compositions and methods for influencing the growth of plants
US3235361A (en) 1962-10-29 1966-02-15 Du Pont Method for the control of undesirable vegetation
US3060084A (en) 1961-06-09 1962-10-23 Du Pont Improved homogeneous, readily dispersed, pesticidal concentrate
US3364229A (en) 1964-01-30 1968-01-16 Shell Oil Co 1, 4 dithiin-2, 3, 5, 6-tetracarboximides and process for their preparation
US3299566A (en) 1964-06-01 1967-01-24 Olin Mathieson Water soluble film containing agricultural chemicals
US3309192A (en) 1964-12-02 1967-03-14 Du Pont Method of controlling seedling weed grasses
US4144050A (en) 1969-02-05 1979-03-13 Hoechst Aktiengesellschaft Micro granules for pesticides and process for their manufacture
US3920442A (en) 1972-09-18 1975-11-18 Du Pont Water-dispersible pesticide aggregates
US4172714A (en) 1976-12-20 1979-10-30 E. I. Du Pont De Nemours And Company Dry compactible, swellable herbicidal compositions and pellets produced therefrom
GB2095558B (en) 1981-03-30 1984-10-24 Avon Packers Ltd Formulation of agricultural chemicals
DE3246493A1 (en) 1982-12-16 1984-06-20 Bayer Ag, 5090 Leverkusen METHOD FOR PRODUCING WATER-DISPERSIBLE GRANULES
US5180587A (en) 1988-06-28 1993-01-19 E. I. Du Pont De Nemours And Company Tablet formulations of pesticides
ES2126553T3 (en) 1989-08-30 1999-04-01 Aeci Ltd DOSING DEVICE AND ITS USE.
CA2083185A1 (en) 1990-03-12 1991-09-13 William Lawrence Geigle Water-dispersible or water-soluble pesticide granules from heat-activated binders
DE69122201T2 (en) 1990-10-11 1997-02-06 Sumitomo Chemical Co Pesticides composition
WO1993019054A1 (en) 1992-03-26 1993-09-30 Dowelanco N-heterocyclic nitro anilines as fungicides
FR2704387B1 (en) 1993-04-28 1995-06-09 Rhone Poulenc Agrochimie CONCENTRATED COMPOSITIONS OF MATERIALS ACTIVE IN AGRICULTURE.
DE4405207A1 (en) 1994-02-18 1995-08-24 Bayer Ag N-pyrazolylanilines and N-pyrazolylaminopyridines
ES2152396T3 (en) 1994-04-06 2001-02-01 Shionogi & Co DERIVED FROM PHENYLACETIC ACID WITH REPLACEMENT IN GAMMA, ITS PROCEDURE FOR OBTAINING AND AGRICULTURAL BACTERICIDE CONTAINING IT.
JPH08208620A (en) 1995-02-03 1996-08-13 Takeda Chem Ind Ltd Aminopyrazole derivative, its production and use
ZA964248B (en) 1995-06-23 1997-11-27 Du Pont Uniform mixtures of pesticidal granules.
WO1998052941A1 (en) 1997-05-22 1998-11-26 G.D. Searle And Co. PYRAZOLE DERIVATIVES AS p38 KINASE INHIBITORS
CA2319807C (en) 1998-02-06 2010-04-06 Meiji Seika Kaisha Ltd. Novel antifungal compound and process for producing the same
HU228503B1 (en) 1999-08-20 2013-03-28 Dow Agrosciences Llc Fungicidal heterocyclic aromatic amides and their compositions, methods of use and preparation
GB9929163D0 (en) * 1999-12-09 2000-02-02 Novartis Ag Organic compounds
DE10136065A1 (en) 2001-07-25 2003-02-13 Bayer Cropscience Ag pyrazolylcarboxanilides
CN1259318C (en) 2001-08-20 2006-06-14 日本曹达株式会社 Tetrazoyl oxime derivative and agrochemical containing the same as active ingredient
TWI283164B (en) 2001-09-21 2007-07-01 Du Pont Anthranilamide arthropodicide treatment
AR037328A1 (en) 2001-10-23 2004-11-03 Dow Agrosciences Llc COMPOSITE OF [7-BENCIL-2,6-DIOXO-1,5-DIOXONAN-3-IL] -4-METOXIPIRIDIN-2-CARBOXAMIDE, COMPOSITION THAT UNDERSTANDS AND METHOD THAT USES IT
GB0227555D0 (en) 2002-11-26 2002-12-31 Syngenta Ltd Fungicides
AR042067A1 (en) 2002-11-27 2005-06-08 Bayer Pharmaceuticals Corp USEFUL ANILINOPIRAZOL DERIVATIVES IN THE TREATMENT OF DIABETES
GB0312863D0 (en) 2003-06-04 2003-07-09 Syngenta Ltd Fungicides
WO2005042474A1 (en) 2003-10-31 2005-05-12 Mitsui Chemicals, Inc. Diamine derivative, process for producing the same, and plant disease control agent containing the same as active ingredient
TWI366438B (en) 2004-08-12 2012-06-21 Ishihara Sangyo Kaisha Fungicidal composition containing acid amide derivative
GB0426372D0 (en) 2004-12-01 2005-01-05 Syngenta Ltd Fungicides
GB0426373D0 (en) 2004-12-01 2005-01-05 Syngenta Ltd Fungicides
EP1912497A1 (en) 2005-08-05 2008-04-23 Basf Se Fungicidal n-[2-(haloalkoxy)phenyl]heteroarylcarboxamides
EP1928455A1 (en) 2005-08-31 2008-06-11 Bayer Healthcare, LLC Anilinopyrazole derivatives useful for the treatment of diabetes
JP5068985B2 (en) 2005-12-16 2012-11-07 石原産業株式会社 Bactericidal composition containing a carboxylic acid amide derivative
TWI372752B (en) 2005-12-22 2012-09-21 Nihon Nohyaku Co Ltd Pyrazinecarboxamide derivatives and plant disease controlling agents containing the same
WO2008013622A2 (en) * 2006-07-27 2008-01-31 E. I. Du Pont De Nemours And Company Fungicidal azocyclic amides
JPWO2008093639A1 (en) 2007-01-29 2010-05-20 武田薬品工業株式会社 Pyrazole compounds
GB0704906D0 (en) 2007-03-14 2007-04-25 Syngenta Participations Ag Fungicides
CL2008001647A1 (en) 2007-06-08 2008-10-10 Syngenta Participations Ag COMPOUNDS DERIVED FROM FENILETIL-AMIDA ACIDO-1H-PIRAZOL-4-CARBOXILICO; COMPOUNDS DERIVED FROM (FENILETIL) AMINA; METHOD TO CONTROL OR PREVENT INFRASTATION OF PLANTS BY PHYTOOPATHOGEN MICROORGANISMS; AND COMPOSITION FOR CONTROL
GB0717260D0 (en) 2007-09-05 2007-10-17 Syngenta Participations Ag Novel fungicides
GB0717258D0 (en) 2007-09-05 2007-10-17 Syngenta Participations Ag Novel fungicides
GB0800407D0 (en) 2008-01-10 2008-02-20 Syngenta Participations Ag Fungicides
DK2562166T3 (en) 2008-01-22 2015-11-23 Dow Agrosciences Llc 5-fluoro-pyrimidine derivatives as fungicides
BRPI0910837B1 (en) 2008-04-30 2017-03-07 Bayer Cropscience Ag thiazole-4-carboxylic esters and thioesters, their uses, and method and composition for controlling harmful phytopathogenic fungi
PE20091953A1 (en) 2008-05-08 2010-01-09 Du Pont SUBSTITUTED AZOLS AS FUNGICIDES
WO2010025451A2 (en) 2008-08-29 2010-03-04 Dow Agrosciences Llc 5,8-difluoro-4-(2-(4-(heteroaryloxy)-phenyl)ethylamino)quinazolines and their use as agrochemicals
AR075713A1 (en) * 2009-03-03 2011-04-20 Du Pont FUNGICIDE PIRAZOLS
AR076839A1 (en) 2009-05-15 2011-07-13 Bayer Cropscience Ag FUNGICIDE DERIVATIVES OF PIRAZOL CARBOXAMIDAS
TR201908611T4 (en) 2009-10-07 2019-07-22 Dow Agrosciences Llc Synergistic fungicidal mixtures containing epoxiconazole for fighting fungus in cereals.
WO2011051243A1 (en) 2009-10-29 2011-05-05 Bayer Cropscience Ag Active compound combinations
WO2012023143A1 (en) * 2010-08-19 2012-02-23 E. I. Du Pont De Nemours And Company Fungicidal pyrazoles
TW201245155A (en) 2010-09-01 2012-11-16 Du Pont Fungicidal pyrazoles

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2010123791A1 (en) * 2009-04-22 2010-10-28 E. I. Du Pont De Nemours And Company Solid forms of an azocyclic amide
WO2012031061A2 (en) * 2010-09-01 2012-03-08 E. I. Du Pont De Nemours And Company Fungicidal pyrazoles and their mixtures

Cited By (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9107412B2 (en) 2010-09-01 2015-08-18 E I Du Pont De Nemours And Company Fungicidal pyrazoles and their mixtures
US9596853B2 (en) 2010-09-01 2017-03-21 E I Du Pont De Nemours And Company Fungicidal pyrazoles and their mixtures
US20160075661A1 (en) * 2013-05-20 2016-03-17 E.I. Du Pont De Nemours And Company Solid forms of fungicidal pyrazoles
US9688639B2 (en) * 2013-05-20 2017-06-27 E I Du Pont De Nemours And Company Solid forms of fungicidal pyrazoles
US10188109B2 (en) 2014-12-30 2019-01-29 Dow Agrosciences Llc Picolinamide compounds with fungicidal activity
US10173981B2 (en) 2014-12-30 2019-01-08 Dow Agrosciences Llc Picolinamides as fungicides
US10173971B2 (en) 2014-12-30 2019-01-08 Dow Agrosciences Llc Picolinamides with fungicidal activity
US10252989B2 (en) 2014-12-30 2019-04-09 Dow Agrosciences Llc Picolinamides with fungicidal activity
US10433555B2 (en) 2014-12-30 2019-10-08 Dow Agrosciences Llc Picolinamide compounds with fungicidal activity
US12114660B2 (en) 2014-12-30 2024-10-15 Corteva Agriscience Llc Picolinamide compounds with fungicidal activity
US10172358B2 (en) 2016-08-30 2019-01-08 Dow Agrosciences Llc Thiopicolinamide compounds with fungicidal activity
US10173982B2 (en) 2016-08-30 2019-01-08 Dow Agrosciences Llc Picolinamides as fungicides
US10214490B2 (en) 2016-08-30 2019-02-26 Dow Agrosciences Llc Picolinamides as fungicides
US10231452B2 (en) 2016-08-30 2019-03-19 Dow Agrosciences Llc Thiopicolinamide compounds with fungicidal activity
US10244754B2 (en) 2016-08-30 2019-04-02 Dow Agrosciences Llc Picolinamide N-oxide compounds with fungicidal activity
US10334852B2 (en) 2016-08-30 2019-07-02 Dow Agrosciences Llc Pyrido-1,3-oxazine-2,4-dione compounds with fungicidal activity
US10246417B2 (en) 2017-01-05 2019-04-02 Dow Agrosciences Llc Picolinamides as fungicides

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